Sizing instrument and punch for use in a surgical procedure to implant a stemless humeral component

ABSTRACT

A stemless humeral component for replacing the humeral head of a patient&#39;s humerus includes a support flange having a number of cantilevered legs extending distally away from a bottom surface thereof. Instruments and methods for surgically installing the stemless humeral component are also disclosed.

This application is a continuation of pending U.S. patent applicationSer. No. 13/803,272, filed Mar. 14, 2013, which claims priority under 35U.S.C. §119 to U.S. Provisional Patent Application Ser. Nos. 61/618,385and 61/618,389, both of which were filed on Mar. 30, 2012. Each of theabove-identified applications is incorporated herein by reference.

CROSS REFERENCE

Cross reference is made to copending U.S. patent application Ser. No.13/803,526 entitled “SURGICAL METHOD FOR IMPLANTING A STEMLESS HUMERALCOMPONENT TO THE HUMERUS OF A PATIENT”; copending U.S. patentapplication Ser. No. 13/803,514 entitled “SIZING INSTRUMENT AND PUNCHFOR USE IN A SURGICAL PROCEDURE TO IMPLANT A STEMLESS HUMERALCOMPONENT”; copending U.S. patent application Ser. No. 13/803,496entitled “DRILL GUIDE FOR USE IN A SURGICAL PROCEDURE TO IMPLANT ASTEMLESS HUMERAL COMPONENT”; and copending U.S. patent application Ser.No. 13/803,533 entitled “IMPLANT INSERTION TOOL FOR USE IN A SURGICALPROCEDURE TO IMPLANT A STEMLESS HUMERAL COMPONENT”, each of which isassigned to the same assignee as the present application, each of whichwas filed on Mar. 14, 2013, and each of which is hereby incorporated byreference.

Cross reference is also made to copending U.S. patent application Ser.No. ______ entitled “SURGICAL METHOD FOR IMPLANTING A STEMLESS HUMERALCOMPONENT TO THE HUMERUS OF A PATIENT” (Attorney Docket No.265280-243726, DEP6440USCNT5); copending U.S. patent application Ser.No. ______ entitled “STEMLESS HUMERAL COMPONENT OF AN ORTHOPAEDICSHOULDER PROSTHESIS” (Attorney Docket No. 265280-243725, DEP6440USCNT4);copending U.S. patent application Ser. No. ______ entitled “STEMLESSHUMERAL COMPONENT OF AN ORTHOPAEDIC SHOULDER PROSTHESIS” (AttorneyDocket No. 265280-243722, DEP6440USCNT1); copending U.S. patentapplication Ser. No. ______ entitled “STEMLESS HUMERAL COMPONENT OF ANORTHOPAEDIC SHOULDER PROSTHESIS” (Attorney Docket No. 265280-243723,DEP6440USCNT2); and copending U.S. patent application Ser. No. ______entitled “STEMLESS HUMERAL COMPONENT OF AN ORTHOPAEDIC SHOULDERPROSTHESIS” (Attorney Docket No. 265280-243724, DEP6440USCNT3), each ofwhich is assigned to the same assignee as the present application, eachof which is filed concurrently herewith, and each of which is herebyincorporated by reference.

TECHNICAL FIELD

The present disclosure relates generally to orthopaedic implants,instruments, and surgical methods, and more particularly to a stemlesshumeral component of an orthopaedic shoulder implant, along with itsassociated surgical instruments and methods.

BACKGROUND

During the lifetime of a patient, it may be necessary to perform ashoulder replacement procedure on the patient as a result of, forexample, disease or trauma. In a shoulder replacement procedure, ahumeral prosthesis is used to replace the natural head of the patient'shumerus. The humeral prosthesis typically includes an elongated stemcomponent that is implanted into the intramedullary canal of thepatient's humerus and a generally hemispherically-shaped prosthetic headcomponent that is secured to the stem component. In some shoulderreplacement procedures, the natural glenoid surface of the scapula maybe resurfaced or otherwise replaced with a glenoid component thatprovides a bearing surface upon which the prosthetic head component ofthe humeral prosthesis articulates.

SUMMARY

According to one aspect, a stemless humeral component is used as asubstitute for a conventional humeral intramedullary stem component. Insuch a way, the stemless humeral component functions as a mountingstructure for a humeral head component, but does so without removal ofbone tissue from the intramedullary canal of the patient's humerus aswould be the case with a conventional humeral stem component.

In an embodiment, the stemless humeral component includes a supportflange having a number of cantilevered legs extending distally away froma bottom surface thereof. Each of the legs may be generally T-shapedwhen viewed from a bottom elevational view.

The stemless humeral component may have a number of viewing windowsformed therein to allow the surgeon to visualize the surgically-preparedhumeral surface (i.e., the surface created by surgically resecting thehumeral head) to ensure the stemless humeral component is fully seatedduring surgical implantation thereof. The stemless humeral component mayhave a number of revision slots formed therein that permit a surgeon topass an osteotome or other cutting instrument to cut or otherwise breakthe bony ongrowth, thereby facilitating removal of the stemless humeralcomponent during a revision procedure.

The stemless humeral component may also include an elongated sleeveextending distally away from the bottom surface of its support flange.The sleeve may have a tapered bore formed therein. A tapered post of thehumeral head component may be inserted into, and thereafter furtherurged into, the tapered bore of the stemless humeral component'selongated sleeve so as to taper lock the humeral head component to thestemless humeral component.

According to another aspect, an impaction handle may be used in asurgical procedure to implant the stemless humeral component. Theimpaction handle includes an attachment mechanism that allows the handleto be secured to a number of different instruments used during asurgical procedure to implant the stemless humeral component.

According to another aspect, an alignment handle may be used in asurgical procedure to implant the stemless humeral component. Like theimpaction handle, the alignment handle includes an attachment mechanismthat allows the handle to be secured to a number of differentinstruments used during a surgical procedure to implant the stemlesshumeral component.

According to another aspect, a sizing instrument may be used in asurgical procedure to implant the stemless humeral component. The sizinginstrument is generally dome-shaped and may be secured to the patient'ssurgically-prepared humeral surface during a procedure to implant thestemless humeral component to function as both a sizing trial and apunch and drill guide.

According to another aspect, a trial head component is used for fitassessment during a surgical procedure to implant the stemless humeralcomponent. It may also function as a trial instrument for the humeralhead component, and, as such, includes a generallyhemispherically-shaped body. The trial head component may also functionas a drill guide for guiding a drill bit used to drill (or pre-drill)the holes in the patient's surgically-prepared humeral surface toreceive the legs of the stemless humeral component.

According to yet another aspect, a surgical punch may be used to punchholes in the patient's surgically-prepared humeral surface to receivethe legs of the stemless humeral component. In an embodiment, thesurgical punch is generally fork-shaped and includes a number of tinesthat correspond in shape, size, and location with the legs of thestemless humeral component.

According to another aspect, a center drill bit may be used tosurgically drill (or pre-drill) a hole in the patient'ssurgically-prepared humeral surface to receive the elongated sleeve ofthe stemless humeral component. A peripheral drill bit, on the otherhand, may be used to drill (or pre-drill) the holes in the patient'ssurgically-prepared humeral surface to receive the legs of the stemlesshumeral component.

According to another aspect, an adjustable head resection guide may beused as a cutting guide to guide the advancement of a bone saw blade toresect the humeral head of the patient. The head resection guide mayinclude an arcuate-shaped, stationary cutting guide secured and amovable cutting guide that is movable in a direction toward and awayfrom the stationary cutting guide. In such a way, the adjustable headresection guide may function as a universally-sized instrument.

According to another aspect, a non-adjustable head resection guide maybe used as a cutting guide to guide the advancement of a bone saw bladeto resect the humeral head of the patient. The head resection guide mayinclude a generally rectangular-shaped base having a circular-shapedring secured thereto. The ring may extend outwardly from the base anddefine a circular-shaped opening. The patient's humeral head may becaptured in the opening during resection thereof.

According to a further aspect, an implant insertion tool may be used tofacilitate implantation of the stemless humeral component into thepatient's surgically-prepared humeral surface. In an embodiment, theimplant insertion tool functions as a “quick connect” instrument havinga locked position in which the stemless humeral component is lockedthereto, and an unlocked position in which the stemless humeralcomponent is released therefrom. In another embodiment, the implantinsertion tool may include a locking rod configured to bethreadingly-engaged with the stemless humeral component. In anotherembodiment, the implant insertion tool may include a threaded end thatis configured to engage the stemless humeral component and an aperturesized to receive a connecting pin of an impaction handle. In yet anotherembodiment, the implant insertion tool may include a locking rodconfigured to be threadingly-engaged with the stemless humeral componentand an aperture sized to receive a connecting pin of an impactionhandle.

According to another aspect, a head impaction tool may be used toimpact, and hence taper lock, the head component to the stemless humeralcomponent. The head impaction tool may include a rounded, concave impactsurface that is sized, shaped, and positioned to closely conform to theconvex, generally hemispherically-shaped outer surface of the headcomponent.

BRIEF DESCRIPTION OF THE DRAWINGS

The detailed description particularly refers to the following figures,in which:

FIG. 1 is a medial perspective view of stemless humeral component;

FIG. 2 is a lateral perspective view of the stemless humeral componentof FIG. 1;

FIG. 3 is a medial elevational view of the stemless humeral component ofFIG. 1;

FIG. 4 is a lateral elevational view of the stemless humeral componentof FIG. 1;

FIG. 5 is an enlarged cross-sectional view of the stemless humeralcomponent taken along the line 5-5 of FIG. 3, as viewed in the directionof the arrows;

FIG. 6 is a perspective view of an impaction handle that may be used ina surgical procedure to implant the stemless humeral component of FIG.1;

FIG. 7 is a cross-sectional view of the impaction handle taken along theline 7-7 of FIG. 6, as viewed in the direction of the arrows;

FIG. 8 is a perspective view of an alignment handle that may be used ina surgical procedure to implant the stemless humeral component of FIG.1;

FIG. 9 is a cross-sectional view of the alignment handle taken along theline 9-9 of FIG. 8, as viewed in the direction of the arrows;

FIG. 10 is a medial perspective view of a sizing instrument that may beused in a surgical procedure to implant the stemless humeral componentof FIG. 1;

FIG. 11 is a lateral perspective view of the sizing component of FIG.10;

FIGS. 12 and 13 are perspective views of a trial head component that maybe used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1;

FIG. 14 is a perspective view of a surgical punch that may be used in asurgical procedure to implant the stemless humeral component of FIG. 1;

FIG. 15 is an elevational view of a center drill that may be used in asurgical procedure to implant the stemless humeral component of FIG. 1;

FIG. 16 is an elevational view of a peripheral drill that may be used ina surgical procedure to implant the stemless humeral component of FIG.1;

FIG. 17 is a perspective view of a head resection guide that may be usedin a surgical procedure to implant the stemless humeral component ofFIG. 1;

FIGS. 18 and 19 are side elevational views of the head resection guideof FIG. 17;

FIGS. 20 and 21 are perspective views of an implant insertion tool thatmay be used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1;

FIG. 22 is an end elevational view of the implant insertion tool ofFIGS. 20 and 21 showing the implant insertion tool positioned in itsunlocked position;

FIG. 23 is a view similar to FIG. 22, but showing the implant insertiontool positioned in its locked position;

FIG. 24 is a fragmentary perspective view of a head impaction tool thatmay be used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1, note that a portion of the head impaction tool hasbeen cut away for clarity of description;

FIGS. 25 and 26 are perspective views showing the head resection guidebeing used to resect the humeral head of a patient's humerus;

FIG. 27 is a perspective view showing the sizing instrument beinginstalled on the patient's resected humeral head by use of the alignmenthandle;

FIG. 28 is a perspective view showing the trial head component installedon the sizing instrument;

FIGS. 29 and 30 are perspective views showing the surgical punch beingused to punch holes in the surgically-prepared surface of the patient'shumerus;

FIGS. 31 and 32 are perspective views showing the surgical drill beingused to drill holes in the surgically-prepared surface of the patient'shumerus;

FIGS. 33 and 34 are perspective views showing the implant insertion toolbeing used to implant the stemless humeral component of FIG. 1 into thesurgically-prepared surface of the patient's humerus;

FIG. 35 is a perspective view showing the head impaction tool being usedto install a head component to the implanted stemless humeral component;

FIG. 36 is a fragmentary cross-sectional view showing the head componentinstalled in the implanted stemless humeral component;

FIG. 37 is a perspective view of another implant insertion tool that maybe used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1;

FIG. 38 is a perspective view of a different implant insertion tool thatmay be used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1;

FIGS. 39 and 40 are perspective views of yet another implant insertiontool that may be used in a surgical procedure to implant the stemlesshumeral component of FIG. 1;

FIGS. 41 and 42 are perspective views of another head resection guidethat may be used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1;

FIG. 43 is a medial perspective view of another embodiment of a stemlesshumeral component;

FIG. 44 is a lateral perspective view of the stemless humeral componentof FIG. 43;

FIG. 45 is a medial perspective view of another embodiment of a sizinginstrument that may be used in a surgical procedure to implant thestemless humeral component of FIG. 1;

FIG. 46 is a lateral perspective view of the sizing component of FIG.45;

FIG. 47 is a perspective view of another embodiment of a surgical punchthat may be used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1;

FIG. 48 is a perspective view of another implant insertion tool that maybe used in a surgical procedure to implant the stemless humeralcomponent of FIG. 1;

FIG. 49 is a perspective view of a drill guide that may be used in asurgical procedure to implant the stemless humeral component of FIG. 1;

FIG. 50 is a top elevation view of the drill guide of FIG. 49;

FIG. 51 is a bottom elevation view of the drill guide of FIG. 49; and

FIG. 52 is a perspective view of another embodiment of a sizinginstrument that may be used in conjunction with the drill guide of FIGS.49-51.

DETAILED DESCRIPTION OF THE DRAWINGS

While the concepts of the present disclosure are susceptible to variousmodifications and alternative forms, specific exemplary embodimentsthereof have been shown by way of example in the drawings and willherein be described in detail. It should be understood, however, thatthere is no intent to limit the concepts of the present disclosure tothe particular forms disclosed, but on the contrary, the intention is tocover all modifications, equivalents, and alternatives falling withinthe spirit and scope of the invention.

Terms representing anatomical references, such as anterior, posterior,medial, lateral, superior, inferior, etcetera, may be used throughoutthis disclosure in reference to both the orthopaedic implants describedherein and a patient's natural anatomy. Such terms have well-understoodmeanings in both the study of anatomy and the field of orthopaedics. Useof such anatomical reference terms in the specification and claims isintended to be consistent with their well-understood meanings unlessnoted otherwise.

Referring now to FIGS. 1-5, there is shown a stemless humeral component10. As will be described in more detail below, the stemless humeralcomponent 10 is used as a substitute for a conventional humeralintramedullary stem component. In such a way, the stemless humeralcomponent 10 functions as a mounting structure for a humeral headcomponent 12 (see FIGS. 35 and 36), but does so without removal of bonetissue from the intramedullary canal of the patient's humerus as wouldbe the case with a conventional humeral stem component.

The stemless humeral component 10 includes a support flange 14 having anumber of legs 16 extending distally away from a bottom surface 18thereof. In the illustrative embodiment described herein, the supportflange 14 is circular in shape. The top surface 20 of the support flange14 includes an annular-shaped, beveled surface 22. An annular ring 24extends around the periphery of the support flange's beveled surface 22.The annular ring 24 has a number of suture holes 26 formed therein. Thesuture holes 26 may be used to suture bone wafers or soft tissue to thestemless humeral component 10. For example, the natural attachment ofthe patient's rotator cuff may be preserved by harvesting a bone waferaround it and then suturing such a bone wafer to the stemless humeralcomponent 10 by use of the suture holes 26.

The support flange's annular ring 24 also has a number of revision slots28 formed therein. As can be seen in FIGS. 1 and 4, one of the revisionslots 28 is positioned on the annular ring 24 at a location above, andradially outwardly from, each of the legs 16. In such a way, anosteotome or other cutting instrument may be passed through the revisionslots to cut or otherwise break the bony ongrowth to the legs 16 therebyfacilitating removal of the stemless humeral component 10 during arevision procedure.

The support flange 14 also has a number of viewing windows 30 formedtherein. The viewing windows 30 allow the surgeon to visualize thesurgically-prepared humeral surface (i.e., the surface created bysurgically resecting the humeral head) to ensure the stemless humeralcomponent 10 is fully seated during surgical implantation thereof. Itshould be appreciated that the viewing windows 30 may also function asadditional revision slots through which the surgeon may pass anosteotome or other cutting instrument slots to cut or otherwise breakthe bony ongrowth to the legs 16 thereby facilitating removal of thestemless humeral component 10 during a revision procedure.

As can be seen in FIGS. 2 and 5, an elongated sleeve 36 extends distallyaway from a bottom surface 18 of the support flange 14 in the samegeneral direction as the legs 16. The sleeve 36 includes a tapereddistal end 38 that functions as a lead-in to facilitate insertion into ahole drilled or otherwise formed in the patient's surgically-preparedhumeral surface (i.e., the surface created by surgically resecting thehumeral head). The elongated sleeve 36 has a tapered bore 40 formedtherein. A tapered post 42 extends laterally out of the backside surfaceof the humeral head component 12 (i.e., the side opposite the humeralhead component's generally hemispherically-shaped outer bearing surface)and is received into the tapered bore 40 of the stemless humeralcomponent's elongated sleeve 36 (see FIG. 36). As will be discussedbelow in greater detail below, urging the tapered post 42 of the humeralhead component 12 into contact with the sidewall defining the taperedbore 40 of the elongated sleeve 36 taper locks the humeral headcomponent 12 to the stemless humeral component 10. As can be seen inFIG. 5, the upper end 44 of the tapered bore 40 opens into the topsurface 20 of the support flange 14, with the lower, distal end 46 ofthe tapered bore 40 opening into a threaded bore 48. The threaded bore48 extends distally away from the distal end 46 of the tapered bore 40and opens into the distal end 38 of the elongated sleeve 36. As can beseen in FIG. 5, a number of threads 50 are formed in the sidewall thatdefines the threaded bore 48. The threads 50 are sized to match, andhence threadingly receive, the threads of an implant retraction tool(not shown) or, as discussed in more detail below, an implant insertiontool.

As can be seen in FIGS. 2, 4, and 5, each of the legs 16 is cantileveredand, as a result, includes one end secured to the bottom surface 18 ofthe support flange 14 with the other end of the leg 16 being free (i.e.,not secured to the support flange 14, any of the other legs 16, or anyother structure of the stemless humeral component 10). As can also beseen in FIGS. 2, 4, and 5, each of the legs 16 is generally T-shapedwhen viewed from a bottom elevational view (i.e., a view that isorthogonal to the longitudinal axis of the leg 16) and, as a result, hasa T-shaped lateral cross section (i.e., a cross section taken in theplane orthogonal to the longitudinal axis of the leg). In such anarrangement, each of the legs 16 has a bone-engaging plate 52 having anumber of serrations 54 formed in a side thereof that faces outwardlyfrom the elongated sleeve 36 (and hence the center of the support flange14). As can be seen best in FIG. 5, each of the serrations 54 is angledupwardly in a direction toward the support flange 14 (i.e., in adirection away from the distal end 56 of the leg 16). When implanted inbone tissue, such upwardly angled serrations 54 engage the bone tissuein a manner that resists pullout of the stemless humeral component 10.An elongated rib 58 extends along the length of the engaging plate 52and, as such, forms the “trunk” of the T-shaped leg 16, with thebone-engaging plate 52 forming its “cross bar”. Specifically, the rib 58is secured to the backside of the leg's engaging plate 52 (i.e., theside opposite the serrations 54) and extends inwardly in the directiontoward the center of the support flange 14. The longitudinal axis of therib 58 is parallel with the longitudinal axis of the engaging plate 52.As can be seen in FIGS. 2 and 5, each of the legs 16 includes a beveleddistal end 62 that functions as a lead-in to facilitate insertion of theleg 16 into a hole punched or otherwise formed in the patient'ssurgically-prepared humeral surface (i.e., the surface created bysurgically resecting the humeral head).

As can be seen best in FIGS. 2 and 4, the bottom surface 18 of thestemless humeral component's support flange 14 has a number of undercuts70 formed therein. In the illustrative embodiment described herein, theundercuts 70 are positioned radially around the elongated sleeve 36about 90° from one another. As can be seen in FIGS. 2 and 4, theposition of the undercuts 70 coincides with the radial position of eachof the viewing windows 30. Specifically, the undercuts 70 are formed inthe same sidewall 72 that defines the radially inner surface of each ofthe viewing windows 30 (i.e., the surface defining the viewing windows30 closest to the center of the stemless humeral component 10). Each ofthe undercuts 70 takes the form of a lip 74 that extends radiallyinwardly into its corresponding viewing window 30. In such anarrangement, as will be discussed below in more detail, the lips 74 ofthe undercuts 70 are positioned to be engaged by a locking pawl of animplant insertion tool.

The stemless humeral component 10 may be constructed with animplant-grade biocompatible metal, although other materials may also beused. Examples of such metals include cobalt, including cobalt alloyssuch as a cobalt chrome alloy, titanium, including titanium alloys suchas a Ti6Al4V alloy, and stainless steel. Such a metallic stemlesshumeral component 10 may also be coated with a surface treatment, suchas hydroxyapatite, to enhance biocompatibility. Moreover, the surfacesof the stemless humeral component 10 that engage the natural bone, suchas the bottom surface 18 of the support flange 14, the outer surfaces ofthe elongated sleeve 36, and the legs 16, may be textured to facilitatesecuring the component to the bone. Such surfaces may also be porouscoated to promote bone ingrowth for permanent fixation.

The stemless humeral component 10 and the head component 12 may beprovided in various different configurations to provide the flexibilitynecessary to conform to varying anatomies from patient to patient. Forexample, the stemless humeral component 10 and the head component 12 maybe provided in various diameters to match the needs of a given patient.It should be appreciated that the head thickness changes with thediameter of the head.

Referring now to FIGS. 6-24, there is shown a set of surgicalinstruments that may be used for the surgical preparation of thepatient's humerus and the subsequent implantation of the stemlesshumeral component 10. The first of such instruments is an impactionhandle 80 shown in FIGS. 6 and 7. As will be described below in moredetail, the impaction handle 80 may be secured to a surgical punch orthe stemless humeral component 10 to facilitate implantation of thestemless humeral component 10 into the patient's surgically-preparedhumeral surface (i.e., the surface created by surgically resecting thehumeral head). The impaction handle 80 includes an elongated body 82having an impact head 84 on one end and an attachment mechanism 86 onits other end. A sleeve 88 is positioned around, and immovably coupledto, the outer surface of the impaction handle's body 82 such as by, forexample, overmolding. The sleeve 88 functions as a grip for allowing thesurgeon to hold the impaction handle 80 during a surgical procedure toimplant the stemless humeral component 10.

The impact head 84 of the impaction handle 80 includes a circular metalplate 90 having an extraction flange 92 extending therefrom. In use, thesurgeon holds the impaction handle 80 via the grip 88 and strikes themetal plate 90 with a surgical mallet, sledge, or other impaction toolto drive the surgical punch 240 (see FIG. 14) or the stemless humeralcomponent 10 into the patient's surgically-prepared humeral surface.

The attachment mechanism 86 of the impaction handle 80 includes a lever94 pivotally coupled to the impaction handle's body 82. The lever 94includes a latching arm 96 and an actuation arm 98 extending at an anglefrom one end of the latching arm 96. A locking pawl 102 is positioned atan opposite end of the latching arm 96 and extends downwardly therefrom.The locking pawl 102 is configured to engage a lip or similar structureformed in one of the surgical instruments described herein (e.g., thesurgical punch or the implant insertion tool) to selectively secure suchinstruments to the impaction handle 80. A connecting pin 104 is formedin the distal end of the impaction handle's body 82. The connecting pin104 extends outwardly from an annular face 106 and has a cross sectionthat substantially matches the shape of the corresponding openingdefined in a number of the surgical instruments described herein (e.g.,the surgical punch or the implant insertion tool). As shown in FIG. 6,the connecting pin 104 is substantially D-shaped in cross section and,as a result, includes a flat face 108.

The latching arm 96 of the lever 94 extends beyond the annular face 106such that the locking pawl 102 is positioned over the connecting pin 104and extends toward its flat face 108. This arrangement permits thelocking pawl 102 to engage a lip or similar structure formed in a numberof the surgical instruments described herein (e.g., the surgical punchor the implant insertion tool) to selectively secure such instruments tothe impaction handle 80.

As shown in FIG. 7, a biasing element, such as spring 110 is coupled tothe lever 94. The spring 110 biases the lever's locking pawl 102 towardthe flat face 108 of the connecting pin 104. In doing so, the bias ofthe spring 110 locks the locking pawl 102, and hence the impactionhandle 80, to a number of the surgical instruments described herein(e.g., the surgical punch or the implant insertion tool). When a surgeonor other user presses down on the lever's actuation arm 98, the biasexerted by the spring 110 is overcome, thereby causing the lever 94 topivot. As the lever 94 is pivoted, the locking pawl 102 is moved in adirection away from the flat face 108 of the connecting pin 104. In sucha way, the impaction handle 80 may be released from the surgicalinstrument to which it is coupled.

The metallic components of impaction handle 80 (e.g., the impacthandle's body 82) may be constructed from a medical-grade metal such asstainless steel, cobalt chrome, or titanium, although other metals oralloys may be used. Moreover, in some embodiments, rigid polymers suchas polyetheretherketone (PEEK) may also be used. The grip 88 may beconstructed from a polymer such as silicone.

Referring now to FIGS. 8 and 9, there is shown an alignment handle 120.As will be described below in more detail, the alignment handle 120 maybe secured to a sizing instrument or cutting guide during a procedure toimplant the stemless humeral component 10 into the patient'ssurgically-prepared humeral surface (i.e., the surface created bysurgically resecting the humeral head). The alignment handle 120includes an elongated body 122 having an attachment mechanism 126 on itsdistal end. A sleeve 128 is positioned around, and immovably coupled to,the outer surface of the impaction handle's body 122 such as by, forexample, overmolding. The sleeve 128 functions as a grip for allowingthe surgeon to hold the alignment handle 120 during a surgical procedureto implant the stemless humeral component 10.

The attachment mechanism 126 of the alignment handle 120 is similar tothe attachment mechanism 86 of the impaction handle 80 and, as such,includes a lever 134 pivotally coupled to the impaction handle's body122. The lever 134 includes a latching arm 136 and an actuation arm 138extending at an angle from one end of the latching arm 136. A lockingpawl 142 is positioned at an opposite end of the latching arm 136 andextends downwardly therefrom. The locking pawl 142 is configured toengage a lip or similar structure formed in the sizing instrument 160(see FIG. 10) to secure the sizing instrument 160 to the alignmenthandle 120. A keying pin 144 is formed in the distal end of thealignment handle's body 122. The keying pin 144 extends outwardly froman annular face 146 and has a cross section that substantially matchesthe shape of the corresponding key-hole shape opening 184 defined in thesizing instrument 160 (see FIG. 10). As shown in FIG. 8, the keying pin144 is key-shaped in cross section and, as a result, includes a roundportion having a rectangular portion secured thereto.

The latching arm 136 of the lever 134 extends beyond the annular face146 such that the locking pawl 142 is positioned over the keying pin 144and extends toward its upper surface. This arrangement permits thelocking pawl 142 to engage a lip or similar structure formed in thesizing instrument 160 (see FIG. 10) to secure the sizing instrument 160to the alignment handle 120.

As shown in FIG. 7, a biasing element, such as spring 150 is coupled tothe lever 134. The spring 150 biases the lever's locking pawl 142 towardthe upper surface of the keying pin 144. In doing so, the bias of thespring 150 locks the locking pawl 142, and hence the alignment handle120, to the sizing instrument 160. When a surgeon or other user pressesdown on the lever's actuation arm 138, the bias exerted by the spring150 is overcome, thereby causing the lever 134 to pivot. As the lever134 is pivoted, the locking pawl 142 is moved in a direction away fromthe upper surface of the keying pin 144. In such a way, the alignmenthandle 120 may be released from the sizing instrument 160.

The metallic components of alignment handle 120 (e.g., the alignmenthandle's body 122) may be constructed from a medical-grade metal such asstainless steel, cobalt chrome, or titanium, although other metals oralloys may be used. Moreover, in some embodiments, rigid polymers suchas polyetheretherketone (PEEK) may also be used. The grip 128 may beconstructed from a polymer such as silicone.

Referring now to FIGS. 10 and 11, there is shown the sizing instrument160. As will be described below in more detail, the sizing instrument160 may be secured to the patient's surgically-prepared humeral surfaceduring a procedure to implant the stemless humeral component 10 tofunction as both a sizing trial and a punch and drill guide.

The sizing instrument 160 includes a generally dome-shaped body 162having flattened upper surface 164 and a substantially planar lowersurface 166. An elongated bore 168 extends through the center of thesizing instrument 160 from its upper surface 164 to its lower surface166. As will be described below in greater detail, the elongated bore168 functions as a drill guide for drilling a hole in the patient'ssurgically-prepared humeral surface to receive the elongated sleeve 36of the stemless humeral component 10 (see FIGS. 2 and 5).

The sizing instrument 160 also includes a number of generallytriangular-shaped punch guide holes 170. As can be seen in FIG. 10, eachof the punch guide holes 170 is located in one of the four quadrants ofthe sizing instrument's round flange 172. As such, each of the punchguide holes 170 is positioned about 90° from one another. As can be seenin FIGS. 2 and 4, the position of the punch guide holes 170 coincideswith the position of the legs 16 of the stemless humeral component 10.As such, the holes 170 function as a punch guide for punching holes inthe patient's surgically-prepared humeral surface to receive the legs 16of the stemless humeral component 10 (see FIG. 29). To that end, theposition of the punch guide holes 170 also coincides with the positionof each of the tines 252 of the surgical punch 240 (see FIG. 14). Assuch, each of the tines 252 may be aligned with, and advanced through,one of the punch guide holes 170. In such a way, the sizing component160 guides the surgeon's use of the surgical punch 240 while surgicallypreparing the patient's humeral surface to receive the legs 16 of thestemless humeral component 10 (see FIG. 29).

As can be seen in FIG. 11, the sizing instrument 160 has a number ofspikes 174 extending downwardly from its lower surface 166. Each of thespikes 174 has a pointed distal tip 176. The spikes 174 are pressed orotherwise driven into the bone tissue of the patient'ssurgically-prepared humeral surface (i.e., the surface created bysurgically resecting the humeral head) to secure the sizing instrument160 in place during its use. A number of pin holes 178 are also formedin the sizing instrument's body 162 near its outer periphery. When asurgeon desires to supplement the attachment functionality of the spikes174, surgical pins (not shown) may be inserted through the pin holes 178to pin the sizing instrument 160 to the bone tissue of the patient'ssurgically-prepared humeral surface (i.e., the surface created bysurgically resecting the humeral head).

Like the stemless humeral component 10, the sizing instrument's flange172 also has a number of viewing windows 180 formed therein. The viewingwindows 180 allow the surgeon to visualize the surgically-preparedhumeral surface (i.e., the surface created by surgically resecting thehumeral head) to ensure the sizing instrument 160 is fully seated duringits use in the surgical procedure.

As can be seen in FIG. 10, the sizing instrument 160 has a connector 182that may be engaged by the attachment mechanism 126 of the alignmenthandle 120 to secure the sizing instrument 160 to the alignment handle120. The connector 182 has a key-hole shaped opening 184 formed therein.The key-hole opening 184 is sized and shaped to receive the keying pin144 formed in the distal end of the alignment handle's body 122. Theconnector 182 also has a channel 186 formed therein. The connector 182has an undercut 188 formed along the length of the channel 186. Theundercut 188 takes the form of a lip 190 positioned at the top of thechannel 186 and extending outwardly into the channel 186. The lip 190 isengaged by the locking pawl 142 of the alignment handle's attachmentmechanism 126 (see FIGS. 8 and 9) to secure the sizing instrument 160 tothe alignment handle 120.

As can be seen in FIG. 10, the connector 182 is confined within thesizing instrument's dome-shaped profile. As will be described below ingreater detail, such an arrangement allows a trial humeral head to beinstalled on the sizing instrument without interference from theconnector 182.

Like the other instruments and implants described herein, the sizinginstrument 160 may be provided in a number of different sizes. Forexample, in the illustrative embodiment described herein, the sizinginstrument 160 may be embodied in different diameters so as to mimic thevarious possible diameters of the stemless humeral component 10.

The sizing instrument 160 may be constructed from a medical-grade metalsuch as stainless steel, cobalt chrome, or titanium, although othermetals or alloys may be used. Moreover, in some embodiments, rigidpolymers such as polyetheretherketone (PEEK) may also be used. Thepolymers may be injection molded as well.

Referring now to FIGS. 12 and 13, there is shown a trial head component210. The trial head component 210 is used for fit assessment during asurgical procedure to implant the stemless humeral component 10 and thehumeral head component 12. In essence, the trial head component 210 isused to ensure proper size selection of the ultimate humeral headcomponent 12 (i.e., the humeral head component 12 that is ultimatelyimplanted in the patient's humerus). As will be discussed below ingreater detail, the trial head component also functions as a drill guidefor guiding a drill bit used to drill (or pre-drill) the holes in thepatient's surgically-prepared humeral surface to receive the legs 16 ofthe stemless humeral component 10 (see FIGS. 31 and 32).

In the illustrative embodiment described herein, the trial headcomponent 210 is embodied as a polymer trial instrument. As such, thetrial head component 210 may be made of any suitable medical-gradepolymeric material. Examples of such polymeric materials includepolyethylene such as polyetheretherketone (PEEK) or acetal. In otherembodiments, the trial head component may be formed from metal.

As a trial instrument for the humeral head component 12, the trial headcomponent 210 includes a generally hemispherically-shaped body 212. Ascan be seen in FIG. 12, trial head component's body 212 includes asmooth, rounded, outer surface 214 that emanates from an annular rim 216that defines the great circle of body's generally hemispherical shape.As can be seen in FIG. 12, the trial head component's body 212 ishollow. A center lug 218 extends downwardly from the center of thebody's concave underside surface 220. The center lug 218 has a number ofannular bands 222 formed in its outer surface 224. As will be describedin greater detail, the trial head component 210 may be installed on thesizing instrument 160 or the stemless humeral component 10 by insertingthe center lug 218 into the sizing instrument's elongated bore 168 orthe stemless humeral component's tapered bore 40. The center lug'sannular bands 222 frictionally engage the stemless humeral component'stapered bore 40 to frictionally secure the center lug, and hence thetrial head component 210 to the stemless humeral component 10.

As can be seen in FIG. 12, the trial head component's body 212 also hasa number of cylindrically-shaped bosses 226 extending downwardly fromthe center of the body's concave underside surface 220. Each of thebosses 226 has a cylindrically-shaped metallic sleeve 228 insert moldedor otherwise positioned therein. The sleeves 228 have an elongated bore230 formed therein, with such bores 230 extending throughout the entirelength of the sleeves 228. The bores 230 function as drill guides forguiding a drill bit used to drill (or pre-drill) the holes in thepatient's surgically-prepared humeral surface to receive the legs 16 ofthe stemless humeral component 10 (see FIGS. 31 and 32). As such, theposition of each of the guide bores 230 coincides with, and is receivedinto, the punch guide holes 170 of the sizing instrument 160 when thetrial head component 210 is secured to the sizing instrument 160 (seeFIG. 28). In particular, when the trial head component 210 is fullyseated on the sizing instrument 160, the distal end of each of thebosses 226 formed in the trial head component 210 is received into acorresponding punch guide hole 170 of the sizing instrument 160 therebyaligning the guide bores 230 in the proper location.

Like the other instruments and implants described herein, the trial headcomponent 210 may be provided in a number of different sizes. Forexample, in the illustrative embodiment described herein, the trial headcomponent 210 may be embodied in different diameters (e.g., 15 mm, 18mm, or 21 mm) so as to mimic a the diameter of the selected humeral headcomponent 12.

Referring now to FIG. 14, there is shown a surgical punch 240 that isused to punch holes in the patient's surgically-prepared humeral surfaceto receive the legs 16 of the stemless humeral component 10 (see FIGS.29 and 30). Similarly to the other instruments described herein, thesurgical punch 240 may be constructed from a medical-grade metal such asstainless steel, cobalt chrome, or titanium, although other metals oralloys may be used. Moreover, in some embodiments, rigid polymers suchas polyetheretherketone (PEEK) may also be used.

The surgical punch 240 is generally fork-shaped and includes a metalbody 242 that includes an attachment shaft 244. The proximal end of theattachment shaft 244 has a D-shaped socket 260 formed therein. TheD-shaped socket 260 is sized, shaped, and positioned to receive theD-shaped connecting pin 104 of the attachment mechanism 86 of theimpaction handle 80 (see FIG. 6). The outer surface of the attachmentshaft 244 has a channel 246 formed therein. The sidewalls of the shaft244 into which the channel 246 is formed define an undercut 248 thatextends along the length of the channel 246. The undercut 248 takes theform of a lip 250 positioned at the top of the channel 246. When theimpaction handle's connecting pin 104 is inserted in the D-shaped socket260 of the surgical punch 240 and thereafter advanced downwardly, thelip 250 is engaged by the locking pawl 102 of the impaction handle'sattachment mechanism 86 (see FIGS. 6 and 7) to secure the surgical punch240 to the impaction handle 80.

At the end of the shaft 244 opposite the channel 246, the surgicalpunch's body 242 includes a number of tines 252. Each of the tines 252is secured to the shaft 244 by a strut 268. The tines 252 function topunch holes in the patient's surgically-prepared humeral surface toreceive the legs 16 of the stemless humeral component 10 (see FIGS. 29and 30) and, as such, correspond in shape, size, and location with thelegs 16 of the stemless humeral component 10. Like the legs 16 of thestemless humeral component 10, each of the surgical punch's tines 252 isgenerally T-shaped when viewed from a bottom elevation view (i.e., aview that is orthogonal to the longitudinal axis of the tine 252). Insuch an arrangement, each of the tines 252 has a bone-shaping plate 254and an elongated rib 256. The elongated rib 256 extends along the lengthof the engaging plate 254 and, as such, forms the “trunk” of theT-shaped tine 252, with the engaging plate 254 forming the “cross bar”of the T-shaped tine 252. Specifically, the outer surface of theengaging plate 254 faces outwardly from the other tines (and hence thelongitudinal axis of the surgical punch), with the rib 256 being securedto the backside of the tine's engaging plate 254 and extending inwardlyin the direction toward the other tines 252. The longitudinal axis ofthe rib 256 is parallel with the longitudinal axis of the engaging plate254. As can be seen in FIG. 14, each of the tines 252 includes a beveleddistal end 258 that functions as a lead punch surface. The beveleddistal end 258 also functions as a lead-in surface to facilitateinsertion of the tine 252 into a pre-drilled hole in the patient'ssurgically-prepared humeral surface.

The position of the tines 252 coincides with the position of the punchguide holes 170 of the sizing instrument 160. As such, the punch guideholes 170 function to guide the advancement of the tines 252 to punchholes in the patient's surgically-prepared humeral surface to receivethe legs 16 of the stemless humeral component 10 (see FIGS. 29 and 30).As such, each of the tines 252 may be aligned with, and advancedthrough, the punch guide holes 170.

The surgical punch's body 242 also includes a center spike 262 extendingdownwardly from the shaft 244 into the area between the tines 252. Thecenter spike 262 is centered on the longitudinal axis of the surgicalpunch 240. The center spike 262 includes a pointed distal tip 264. Thetip 264 of the center spike 262 makes a divot in the patient'ssurgically-prepared humeral surface during use of the surgical punch 240to punch holes to receive the legs 16 of the stemless humeral component10. Such a divot is positioned to receive the elongated sleeve 36 of thestemless humeral component 10.

Referring now to FIGS. 15 and 16, there is shown a center drill bit 270and a peripheral drill bit 272. The center drill bit 270 is used tosurgically drill a hole in the patient's surgically-prepared humeralsurface to receive the elongated sleeve 36 of the stemless humeralcomponent 10. The peripheral drill bit 272, on the other hand, is usedto drill (or pre-drill) the holes in the patient's surgically-preparedhumeral surface to receive the legs 16 of the stemless humeral component10 (see FIGS. 31 and 32). Each of the drill bits 270, 272 includes anelongated shank 274 having a proximal end 276 that fits into the chuckof a rotary power tool (not shown) or a manual handle (not shown). Thedrill bits 270, 272 also include a cutting head 278 located at theopposite, distal end of the shank 274. The cutting head 278 of the drillbits 270, 272 includes a sharp cutting tip 280 with a plurality ofhelical cutting flutes 282 extending therefrom.

Each of the drill bits 270, 272 also includes an annular collar 284positioned above the cutting head 278 at the upper end of the cuttingflutes 282. The collar 284 functions as a depth stop to ensure the drillbits 270, 272 drill their respective holes at the desired depths. In thecase of the center drill bit 270, the collar has an outer diameter thatis larger than the diameter of the elongated bore 168 of the sizinginstrument 160. Hence, the center drill bit 270 may be advanced into thebone tissue until the lower surface 286 of the collar 284 bottoms out orotherwise engages the flattened upper surface 164 of the sizinginstrument 160. Likewise, the peripheral drill bit 272 may be advancedinto the bone tissue until the lower surface 286 of the collar 284bottoms out or otherwise engages a rim or shelf within the sleeves 228of the trial head component 210.

The drill bits 270, 272 may be constructed from a medical-grade metalsuch as stainless steel, cobalt chrome, or titanium, although othermetals or alloys may be used. Moreover, in some embodiments, rigidpolymers such as polyetheretherketone (PEEK) may also be used.

Referring now to FIGS. 17-19, there is shown a head resection guide 290.The head resection guide 290 is used as a cutting guide to guide theadvancement of a bone saw blade to resect the humeral head of thepatient. The head resection guide 290 includes a base 292 having a pairof rails 294 extending outwardly therefrom. An arcuate-shaped,stationary cutting guide 296 is secured to the end of the rails 296opposite the base 292. Specifically, one end of the stationary cuttingguide 296 is secured to one of the rails 294, with the other end of thestationary cutting guide 296 being secured to the other rail 294.

A movable cutting guide 298 is captured on the rails 294 and is movableback and forth along the rails 294. Specifically, the movable cuttingguide 298 includes a guide body 302 having a pair of holes 304 formedtherein. One of the guide rails 294 is positioned in one of the holes304, with the other rail 294 being positioned in the other hole 304. Assuch, the movable cutting guide 298 may be moved along the rails 294 ina direction toward and away from the stationary cutting guide 296.

A biasing element, such as a coiled spring 306, is captured on each ofthe rails 294. The springs 306 are positioned between an upper surface308 of the base 292 and the lower surface 310 of the movable cuttingguide's body 302. As such, the springs 306 assert a spring bias on themovable cutting guide 298 so as to urge it in the direction toward thestationary cutting guide 296.

The movable cutting guide's body 302 also has a finger grip 312 formedtherein. In the illustrative embodiment described herein, the fingergrip 312 is embodied as a flange extending outwardly in a direction thatis generally orthogonal to the rails 294. A surgeon or other user maygrip the finger grip 312 and the lower surface 314 of the base 292 andthereafter squeeze his or her fingers. Doing so overcomes the springbias of the springs 306 and urges or otherwise moves the movable cuttingguide 298 in the direction away from the stationary cutting guide 296(i.e., in a direction toward the base 292). Once the surgeon releasesthe finger grip 312, the spring bias of the springs 306 urges orotherwise moves the movable cutting guide 298 in the direction away backtoward the stationary cutting guide 296 (i.e., in a direction away fromthe base 292).

As can be seen best in FIG. 18, both the stationary cutting guide 296and the movable cutting guide 298 include rounded surfaces thatcooperate to define a circular-shaped surface for capturing thepatient's humeral head therein. Specifically, the stationary cuttingguide 296 includes a rounded, generally semicircular-shaped posteriorsurface 318 that faces an rounded, generally semicircular-shapedanterior surface 320 of the movable cutting guide 298. As can be seen inFIGS. 17 and 18, a number of spikes 322 extend outwardly from each ofthe semicircular-shaped surfaces 318, 320 toward the oppositesemicircular-shaped surface 318, 320. The spikes 322 engage the bonetissue of the patient's humerus to maintain the head resection guide 290in a desired location and orientation during its use. As such, when asurgeon squeezes the finger grip 312 and the lower surface 314 of thebase 292, the semicircular-shaped surfaces 318, 320 are moved away fromone another thereby creating clearance to position the patient's humeralhead between them. Thereafter, when the surgeon releases the finger grip312 and the lower surface 314 of the base 292, the semicircular-shapedsurfaces 318, 320 are toward one another thereby capturing the patient'shumeral head therebetween with the spikes 322.

As can be seen in FIGS. 17 and 18, the movable cutting guide 298 has anumber of pin holes 324 formed therein. The axis of each of the pinholes 324 extends in a direction that is oblique or angled relative tothe rails 294 and the spikes 322. As will be discussed in more detail,surgical pins may be inserted through the pin holes 324 to pin the headresection guide 290 to the patient's humerus during resection of thepatient's natural humeral head.

As can be seen best in the side view of FIG. 19, both the stationarycutting guide 296 and the movable cutting guide 298 include planarsurfaces that cooperate to define a cutting guide surface for guiding abone saw blade to resect the patient's natural humeral head.Specifically, the stationary cutting guide 296 includes a planarposterior guide surface 326 that aligns in a coplanar relationship witha planar anterior guide surface 328 of the movable cutting guide 298.Collectively, the two guide surfaces 326, 328 define a cutting surfaceupon which a bone saw blade may be supported (i.e., guided) during acutting operation to resect the patient's natural humeral head. As canbe seen in FIG. 19, the two guide surfaces 326, 328 lie in a plane thatis generally parallel to the rails 294 and perpendicular to the fingergrip 312 and the lower surface 314 of the base 292.

The head resection guide 290 may be constructed from a medical-grademetal such as stainless steel, cobalt chrome, or titanium, althoughother metals or alloys may be used. Moreover, in some embodiments, rigidpolymers such as polyetheretherketone (PEEK) may also be used.

Referring now to FIGS. 20-23, there is shown an implant insertion tool330. The implant insertion tool 330 may be secured to the stemlesshumeral component 10 to facilitate implantation of the stemless humeralcomponent 10 into the patient's surgically-prepared humeral surface. Theimplant insertion tool 330 includes an elongated body 332 that defines acylindrically-shaped shaft 334 having a connector 336 on its proximalend. The connector 336 includes a D-shaped socket 338 formed in itsproximal end. The D-shaped socket 338 is sized, shaped, and positionedto receive the D-shaped connecting pin 104 of the attachment mechanism86 of the impaction handle 80 (see FIG. 6). The outer surface of thebody's connector 336 has a channel 340 formed therein. The sidewalls ofthe connector 336 into which the channel 340 is formed define anundercut 342 that extends along the length of the channel 340. Theundercut 342 takes the form of a lip 344 positioned at the top of thechannel 340. When the impaction handle's connecting pin 104 is insertedin the D-shaped socket 338 of the implant insertion tool 330 andthereafter advanced downwardly, the lip 344 is engaged by the lockingpawl 102 of the impaction handle's attachment mechanism 86 (see FIGS. 6and 7) to secure the implant insertion tool 330 to the impaction handle80.

The end of the of the implant insertion tool's body 332 opposite itsconnector 336 has an alignment flange 346 formed therein. The alignmentflange 346 is embodied as an annular face having a number of protrusionsor alignment keys 348 extending downwardly therefrom. The alignment keys348 are sized, shaped, and positioned to be received into the viewingwindows 30 formed in the stemless humeral component 10. The alignmentflange 346 also has an alignment pin 350 extending downwardly from itsannular face. The alignment pin 350 is sized, shaped, and positioned tobe received into the tapered bore 40 formed in the stemless humeralcomponent 10.

As can be seen in FIGS. 20 and 21, a pair of locking arms 352 arepivotally coupled to the insertion tool's body 332. Each of the lockingarms 352 has a cam follower 354 formed in its proximal end, and agenerally L-shaped locking pawl 356 formed in its opposite, distal end.Each of the locking arms 352 is pivotally coupled to the implantinsertion tool's body 332 at a location near its annular face 346 by apivot pin 358 positioned in a bore 360 formed in the body 332. Thelocking arms 352 pivot about the pivot pins 358 such that movement ofthe cam followers 354 in the direction toward one another, and hencetoward the shaft 334 of the insertion tool's body 332, causes movementof the locking pawls 356 in the direction away from one another, andhence away from the alignment pin 350 of the insertion tool's body 332.On the other hand, movement of the cam followers 354 in the directionaway from one another, and hence away from the shaft 334 of theinsertion tool's body 332, causes movement of the locking pawls 356 inthe direction toward one another, and hence toward the alignment pin 350of the insertion tool's body 332.

Such movement of the locking arms 352 may be used as part of a “quickconnect” arrangement to selectively lock and release the stemlesshumeral component 10 from the implant insertion tool 330. In particular,when the insertion tool's alignment flange 346 is engaged with thestemless humeral component 10 such that its alignment pin 350 andalignment keys 348 are positioned in the stemless humeral component'stapered bore 40 and viewing windows 30, respectively, the locking pawls356 of the locking arms 352 are positioned in the stemless humeralcomponent's remaining viewing windows 30 (i.e., the viewing windows 30not occupied by the alignment keys 348). So positioned, the lockingpawls 356 may be moved into and out of engagement with the lips 74 ofthe undercuts 70 formed in the bottom surface 18 of the stemless humeralcomponent's support flange 14 (see FIGS. 2 and 4). Specifically, thelocking pawls 356 may be moved in the direction toward one another(i.e., toward the alignment pin 350 of the insertion tool's body 332)such that the locking pawls 356 engage the lips 74 of the undercuts 70formed in the bottom surface 18 of the stemless humeral component'ssupport flange 14 thereby securing the stemless humeral component 10 tothe implant insertion tool 330. Oppositely, the locking pawls 356 may bemoved in the direction away from one another (i.e., away from thealignment pin 350 of the insertion tool's body 332) such that thelocking pawls 356 disengage the lips 74 of the undercuts 70 formed inthe bottom surface 18 of the stemless humeral component's support flange14 thereby releasing the stemless humeral component 10 from the implantinsertion tool 330.

As can be seen in FIGS. 20 and 21, a rotating locking collar 362 iscaptured on the shaft 334 of the insertion tool's body 332. Inparticular, the locking collar 362 has a bore 364 extending through itscenter, with the shaft 334 of the insertion tool's body 332 beingreceived (i.e., positioned) in the bore 364. As such, the locking collar362 may be rotated both clockwise and counterclockwise about the shaft334 of the insertion tool's body 332. As can be seen best in FIG. 20,the locking collar 362 has a pair of channels 366 formed in itsunderside. The cam followers 354 of the locking arms 352 ride in thechannels 366 as the locking collar 362 is rotated about the shaft 334.The sidewall defining the inner side of the channels 366 defines a camsurface 368. As can be seen in FIG. 20, one end 370 of the cam surface368 is nearer the locking collar's bore 364 (and hence the shaft 334 ofthe insertion tool's body 332) than the other end 372 of the cam surface368. As such, as each of the cam followers 354 rides along itscorresponding cam surface 368 in the direction from its inner end 370 toits outer end 372, the cam followers 354 move in the direction away fromone another, and hence away from the shaft 334 of the insertion tool'sbody 332, thereby causing the locking arms 352 to pivot such that thelocking pawls 356 are moved in a direction toward one another, and hencetoward the alignment pin 350 of the insertion tool's body 332. Asdescribed above, such movement of the locking pawls 356 is used to lockthe stemless humeral component 10 to the implant insertion tool 330. Ascan be seen in FIG. 20, in the illustrative embodiment described herein,clockwise rotation of the locking collar 362 causes the cam followers354 to move along the cam surfaces 368 in such a direction (i.e., in adirection from the cam surface's inner end 370 to its outer end 372).

Oppositely, as each of the cam followers 354 rides along thecorresponding cam surface 368 in the direction from its outer end 372 toits inner end 370, the cam followers 354 move in the direction towardone another, and hence toward the shaft 334 of the insertion tool's body332, thereby causing the locking arms 352 to pivot such that the lockingpawls 356 are moved in a direction away from one another, and hence awayfrom the alignment pin 350 of the insertion tool's body 332. Asdescribed above, such movement of the locking pawls 356 is used torelease the stemless humeral component 10 from the implant insertiontool 330. As can be seen in FIG. 20, in the illustrative embodimentdescribed herein, counterclockwise rotation of the locking collar 362causes the cam followers 354 to move along the cam surfaces 368 in sucha direction (i.e., in a direction from the cam surface's outer end 372to its inner end 370).

As can be seen in FIGS. 20 and 21, the locking collar 362 has a pair ofguide pins 374 extending therethrough. The outer end of the guide pins374 is positioned near the outer surface of the locking collar 362, withits inner end (not shown) positioned in an annular channel (not shown)formed on the outer surface of the shaft 334 of the insertion tool'sbody 332. The inner end of the guide pins 374 rides in such a channelduring rotation of the locking collar 362. The shaft 334 of theinsertion tool's body 332 also has a pair of linear channels 376 formedin its outer surface. The linear channels 376 are arranged parallel toboth one another and the longitudinal axis of the shaft 334 of theinsertion tool's body 332. When the inner ends of the guide pins 374 arealigned with, and received into, the linear channels 376, the lockingcollar 362 may be slid along the shaft 334 of the insertion tool's body332 in the direction toward the connector 336 (i.e., away from thealignment flange 346). In doing so, each of the cam followers 352 of thelocking arms 350 escape from their respective channels 366 of thelocking collar 362. Such an arrangement allows the cam followers 352 andthe channels 366 of the locking collar 362 to be fully exposed tocleaning fluid during cleaning of the implant insertion tool 330 betweenuses. The cam followers 352 may be slipped back into their respectivechannels 366 of the locking collar 362 by aligning them with the innerends 370 of channels 366 as the locking collar 362 is slid along theshaft 334 of the insertion tool's body 332 in the direction away fromthe connector 336 (i.e., toward the alignment flange 346). Thereafter,the locking collar 362 may be rotated to recapture the cam followers 352in their respective channels 366 of the locking collar 362.

The components of the implant insertion tool 330 (e.g., its body 332,locking arms 352, and locking collar 362) may be constructed from amedical-grade metal such as stainless steel, cobalt chrome, or titanium,although other metals or alloys may be used. Moreover, in someembodiments, rigid polymers such as polyetheretherketone (PEEK) may alsobe used.

Referring now to FIG. 24, there is shown an head impaction tool 380. Thehead impaction tool 380 may be used to impact, and hence taper lock, thehead component 12 to the stemless humeral component 10. The headimpaction tool 380 includes a generally conically-shaped body 382 havinga connector 384 formed in its proximal end. The connector 384 includes around opening 386 that is sized, shaped, and positioned to receive theconnecting pin 104 of the attachment mechanism 86 of the impactionhandle 80 (see FIG. 6). The connector 384 of the head impaction tool 380also has three channels 388 formed therein. The sidewalls of the headimpaction tool's body 382 into which the channels 388 are formed defineundercuts 390 that extend along the length of the channels 388. Each ofthe undercuts 390 takes the form of a lip 392 positioned at the top ofthe respective channels 388. The lips 392 may be selectively engaged bythe locking pawl 102 of the impaction handle's attachment mechanism 86(see FIGS. 6 and 7) to secure head impaction tool 380 to the impactionhandle 80.

The end of the head impaction tool's body 382 opposite the connector 384has a rounded, concave impact surface 396 formed therein. The concaveimpact surface 396 is sized, shaped, and positioned to closely conformto the convex, nearly generally hemispherically-shaped outer surface ofthe head component 12. As will be described below in greater detail inregard to FIG. 35, when installing the head component 12 to the stemlesshumeral component 10, the head impaction tool 380 is first coupled tothe impaction handle 80 and thereafter positioned such that the impactsurface 396 of the head impaction tool 380 is placed in contact with theouter surface of the head component 12. The surgeon may then strike theimpact handle's metal strike plate 90 with a surgical mallet, sledge, orother impaction tool to drive the head component 12 into taper lockattachment to the stemless humeral component 10. It should beappreciated that the head impaction tool 380 may be constructed from apolymer such as polyetheretherketone (PEEK), acetal, radel, or otherpolymer.

Referring now to FIGS. 25-36, there is shown a surgical procedure inwhich the various instruments described herein in regard to FIGS. 6-24are used to surgically prepare the patient's humerus 400 forimplantation of the stemless humeral prosthesis 10 of FIGS. 1-5. Thesurgical procedure begins with preoperative planning in which, amongstother things, a CT scan (2D or 3D) or other type of preoperative image(e.g., X-ray) may be obtained to plan the placement location andorientation of the stemless humeral component 10 and humeral headcomponent. If the procedure being planned is a shoulder replacementprocedure, the CT scan or other type of preoperative images will also beused to plan the placement location and orientation of a prostheticglenoid component (not shown) to be implanted in the patient's glenoid.With the preoperative planning complete, the patient's soft tissue isdissected and retracted in order to allow access to the shoulder joint.Full (i.e., 360°) exposure of the patient's humeral head 402 istypically achieved.

Once the patient's humeral head 402 has been surgically exposed, thesurgeon may then begin the process of resecting it. As shown in FIG. 25,the surgeon first installs the head resection guide 290 on the patient'shumerus 400. To do so, the surgeon grips the finger grip 312 and thelower surface 314 of the head resection guide's base 292 and thereaftersqueezes his or her fingers. Doing so overcomes the spring bias of thesprings 306 and urges or otherwise moves the movable cutting guide 298in the direction away from the stationary cutting guide 296 (i.e., in adirection toward the base 292) thereby creating clearance to positionthe patient's humeral head 402 between their respectivesemicircular-shaped surfaces 318, 320.

The surgeon then positions the head resection guide 290 around thepatient's humeral head 402 such that the stationary cutting guide 296rests on the posterior cuff insertion site of the patient's rotatorcuff. Doing so protects the posterior rotator cuff during head resectionand is a step in placing the guide 296 at the correct height andversion. The surgeon then positions the anterior surface 320 of themovable cutting guide 298 against the anterior surface 404 of thepatient's humerus 400 at the desired resection angle and height. Thesurgeon positions cutting guide 298 on the patient's humeral head 402such that the anterior guide surface 328 is aligned with the articularmargin of the humeral head 402. The surgeon then gently releases thefinger grip 312 and the lower surface 314 of the base 292. In doing so,the respective semicircular-shaped surfaces 318, 320 of the movablecutting guide 298 and the stationary cutting guide 296 are moved towardone another thereby capturing the patient's humeral head 402therebetween with the spikes 322.

Once the surgeon has placed the movable cutting guide 298 in the desiredresection angle and height, the surgeon may insert a surgical pin 406through each of the pin holes 324 to pin the head resection guide 290 tothe patient's humerus 400 to maintain the anterior guide surface 328 ofthe movable cutting guide 298 in its desired position, as shown in FIG.25.

As shown in FIG. 26, the surgeon then operates a bone saw, such as anoscillating power saw 408, to resect the patient's humeral head 402. Todo so, the surgeon positions the saw blade 410 of the power saw 408 onthe planar anterior guide surface 328 of the movable cutting guide 298.The surgeon then actuates the oscillating power saw 408 and appliespressure on it so that it advances posteriorly and into contact with theanterior surface 404 of the patient's humerus 400. As the saw blade 410is advanced posteriorly into contact with the anterior surface 404 ofthe humerus 400 and thereafter through its midsection in the directiontoward its posterior surface 412, the oscillating motion of the bone saw408 abrades the bone tissue of the humeral head 402.

The surgeon continues to posteriorly advance the power saw 408 until thesaw blade 410 exits the bone. Specifically, the surgeon continues tooperate the bone saw 408 until the distal tine of its blade 410 passesbeyond the posterior surface 412 of the humeral head 402. Upon exit fromthe posterior surface 412 of the bone, the saw blade 410 is supportedand guided by the posterior guide surface 326 of the stationary cuttingguide 296. In such a way, the posterior guide surface 326 of thestationary cutting guide 296 prevents the saw blade 410 from contactingthe patient's posterior rotator cuff. Once the saw blade 410 has exitedthe bone and advanced onto the posterior guide surface 326 of thestationary cutting guide 296, the surgeon may deactuate the bone saw 408and thereafter then lift away the resected portion of the patient'shumeral head 402. As can be seen in FIG. 26, the surgically resectedsurface 414 of the humerus 400 is substantially planar.

As shown in FIG. 27, the surgeon now determines the appropriate sizestemless humeral component 10 to implant on the surgically resectedsurface 414 of the humerus 400. To do so, the surgeon uses the sizinginstrument 160. Specifically, as will now be described in more detail,the sizing instrument 160 may be secured to the patient's surgicallyresected surface 414 of the humerus 400 to function as both a sizingtrial and a punch and drill guide. To do so, the surgeon selects aninitial one of the differently-sized sizing instruments 160 that thesurgeon estimates is the proper size for the patient. The surgeon thencouples the selected sizing instrument 160 to the alignment handle 120.Specifically, the surgeon inserts and advances the keying pin 144 formedin the distal end of the alignment handle's body 122 into the key-holeshaped opening 184 formed in the sizing instrument 160 until the lip 190of the sizing instrument's connector 182 is engaged by the locking pawl142 of the alignment handle's attachment mechanism 126 (see FIGS. 8 and9) thereby securing the sizing instrument 160 to the alignment handle120. The surgeon then places the selected sizing instrument 160 onto thesurgically resected surface 414 of the humerus 400 and assessescoverage. If the surgeon determines the selected sizing instrument 160is not the proper size, the initial sizing instrument 160 is removed anda sizing instrument 160 having a different diameter is attached to thealignment handle 120 and assessed.

Once the sizing instrument 160 of the proper diameter has beendetermined, the surgeon secures the sizing instrument 160 to thesurgically resected surface 414 of the humerus 400. To do so, thesurgeon utilizes the alignment handle 120 to position the sizinginstrument 160 in a desired location and orientation for the finalimplant (i.e., the stemless humeral component 10) with the spikes 174 ofthe sizing instrument 160 facing downwardly toward the surgicallyresected surface 414 of the humerus 400. The surgeon then presses orotherwise urges the sizing instrument 160 downwardly into the cancellousbone of the surgically-resected surface 414 of the humerus 400 therebysecuring it in place as shown in FIG. 27. The surgeon may utilize thesizing instrument's viewing windows 180 to visualize thesurgically-resected surface 414 of the humerus 400 to ensure the sizinginstrument 160 is fully seated thereon.

Once the sizing instrument 160 has been installed on the surgicallyresected surface 414 of the humerus 400, the surgeon may then perform apre-trial of the fit of the final humeral head component 12. To do so,the surgeon selects an initial one of the differently-sized trial headcomponents 210 that the surgeon estimates is the proper size for thepatient and thereafter installs the selected trial head component 210 tothe sizing instrument 160 (see FIG. 28). The surgeon installs the trialhead component 210 on the sizing instrument 160 by inserting its centerlug 218 (see FIGS. 12 and 13) into the sizing instrument's elongatedbore 168 and thereafter pressing or otherwise urging the trial headcomponent 210 downwardly until it fully seats on the sizing instrument160.

The trial head component 210 is used to ensure proper size selection ofthe ultimate humeral head component 12 (i.e., the humeral head component12 that is ultimately implanted in the patient's humerus). As such, oncethe trial head component 210 is installed on the sizing instrument 160,the surgeon can visually assess its size and fit to get a sense of thesize and fit of the final implant (i.e., the stemless humeral component10 and the humeral head component 12). If the surgeon is not satisfiedwith the assessed size and fit, either one or both of the trial headcomponent 210 and the sizing instrument 160 may be replaced. If thesurgeon is satisfied with the assessed size and fit, the trial headcomponent 210 is removed from the sizing instrument 160 and subsequentbone preparation of the patient's surgically resected humeral surface414 is performed.

As shown in FIG. 29, the surgeon may then use the surgical punch 240 topunch holes in the patient's surgically-resected humeral surface 414 toreceive the legs 16 and the elongated sleeve 36 of the stemless humeralcomponent 10. It should be appreciated that the surgeon may utilize anumber of fixation pins (not shown) inserted through the pin holes 178to secure the sizing instrument 160 to the bone tissue of the patient'ssurgically-resected humeral surface 414 prior to use of the surgicalpunch 240. To perform the punching procedure, the surgeon first securesthe surgical punch 240 to the impaction handle 80 by inserting theD-shaped connecting pin 104 into the D-shaped socket 260 formed in theattachment shaft 244 of the surgical punch 240 until the lip 250 formedin the attachment shaft 244 is engaged by the locking pawl 102 of theimpaction handle's attachment mechanism 86 (see FIGS. 6 and 7) to securethe surgical punch 240 to the impaction handle 80.

Thereafter, the surgeon uses the impaction handle 80 to position thesurgical punch 240 such that each of its tines 252 is aligned with oneof the punch guide holes 170 of the sizing instrument 160. Doing so alsoaligns the surgical punch's center spike 262 with the elongated bore 168of the sizing instrument 160. In such a way, the punch guide holes 170and the elongated bore 168 function to guide the advancement of thetines 252 and the center spike 262, respectively.

Once the surgical punch 240 is positioned in the sizing instrument 160in such a manner, the surgeon strikes the metal plate 90 of theimpaction handle 80 with a surgical mallet, sledge, or other impactiontool to drive the surgical punch 240 into the patient'ssurgically-resected humeral surface 414 until the surgical punch bottomsout on the sizing instrument 160. As shown in FIG. 30, doing so createsa number of punched holes 416 in the patient's surgically-resectedhumeral surface 414 corresponding in shape, size, and location with thelegs 16 of the stemless humeral component 12. As also shown in FIG. 30,impacting the surgical punch 240 in such a manner also creates a recessin the form of a divot 418 in the patient's surgically-resected humeralsurface 414 corresponding in shape, size, and location to the elongatedsleeve 36 of the stemless humeral component 10.

The surgeon then backs out the surgical punch 240 from the patient'ssurgically-resected humeral surface 414 to expose the surgically createdholes 416 and divot 418, as shown in FIG. 30. If necessary, the surgeonmay strike the underside of the impaction handle's extraction flange 92to facilitate such extraction of the surgical punch 240.

Referring now to FIGS. 31 and 32, there is shown a pre-conditioningprocedure to the punching procedure described in regard to FIGS. 29 and30. In other words, the drilling procedure may be performed as apre-drilling procedure in which holes are pre-drilled in the patient'ssurgically-prepared humeral surface 414, with such pre-drilled holesthen being punched by use of the surgical punch 240 in the mannerdescribed above to receive the legs 16 of the stemless humeral component10. To perform such a drilling procedure, the surgeon utilizes the trialhead component 210 with the installed sizing instrument 160. In bonepreparation (as opposed to trialing), the trial head component 210 isused as a drill guide for guiding drill bits used to drill (orpre-drill) holes in the patient's surgically-prepared humeral surface414 to receive the legs 16 and the elongated sleeve 36 of the stemlesshumeral component 10. To begin such a drilling procedure, the surgeonfirst selects the trial head component 210 corresponding in size to theinstalled sizing instrument 160 and thereafter installs the selectedtrial head component 210 to the sizing instrument 160 (see FIG. 31). Thesurgeon installs the trial head component 210 on the sizing instrument160 by inserting its center lug 218 (see FIGS. 12 and 13) into thesizing instrument's elongated bore 168 and thereafter pressing orotherwise urging the trial head component 210 downwardly until it fullyseats on the sizing instrument 160.

When the trial head component 210 is installed to the sizing instrument160, the position of each of the trial head component's guide bores 230coincides with, and is received into, the punch guide holes 170 of thesizing instrument 160. In particular, when the trial head component 210is fully seated on the sizing instrument 160, the distal end of each ofthe bosses 226 formed in the trial head component 210 (see FIGS. 12 and13) is received into a corresponding punch guide hole 170 of the sizinginstrument 160 thereby aligning the guide bores 230 in the properlocation.

The proximal end of the peripheral drill bit 272 is then inserted intothe chuck of a rotary power tool (not shown) or a manual handle (notshown). The surgeon then inserts the tip 280 of the peripheral drillbit's cutting head 278 into one of the guide bores 230 of the trial headcomponent 210 and actuates the power drill (or turns the manual handle).The surgeon advances the peripheral drill bit 272 into the bone tissueof the patient's surgically-resected humeral surface 414 until the lowersurface 286 of the bit's collar 284 bottoms out or otherwise engages therim or shelf in the sleeve 228 of the trial head component 210. Thesurgeon then removes the drill bit 272 from the guide bore 230corresponding to the newly drilled peripheral hole and repeats theprocess in the remaining guide bores 230. The surgeon then removes thetrial head component 210 from the sizing instrument 160 to expose thesurgically-drilled peripheral holes 420 corresponding in location towhere the legs 16 of the stemless humeral component 10 (see FIG. 32)will be implanted.

With the trial head component 210 removed, the surgeon then drills ahole in the patient's surgically-resected humeral surface 414 to receivethe elongated sleeve 36 of the stemless humeral component 10. To do so,the surgeon secures the proximal end of the center drill bit 270 in thechuck of a rotary power tool (not shown) or a manual handle (not shown).The surgeon then inserts the tip 280 of the center drill bit's cuttinghead 278 into the elongated bore 168 of the sizing instrument 160 andactuates the power drill (or turns the manual handle). The surgeonadvances the center drill bit 270 into the bone tissue of the patient'ssurgically-resected humeral surface 414 until the lower surface 286 ofthe bit's collar 284 bottoms out or otherwise engages the flattenedupper surface 164 of the sizing instrument 160. The surgeon then removesthe drill bit 270 from the elongated bore 168 of the sizing instrument160.

As shown in FIG. 32, the surgeon then removes the sizing instrument 160to expose the surgically-drilled peripheral holes 420 corresponding inlocation to where the legs 16 of the stemless humeral component 10 willbe implanted, along with the surgically-drilled center hole 422corresponding in location to where the elongated sleeve 36 of thestemless humeral component 10 will be implanted.

Once the patient's surgically-resected humeral surface 414 has beenprepared, the surgeon may then implant the stemless humeral component10. To do so, as shown in FIG. 33, the surgeon first secures the implantinsertion tool 330 to the impaction handle 80 by inserting the handle'sD-shaped connecting pin 104 into the D-shaped socket 338 of the implantinsertion tool's connector 336 until the connector's lip 344 is engagedby the locking pawl 102 of the impaction handle's attachment mechanism86 (see FIGS. 6 and 7) to secure the implant insertion tool 330 to theimpaction handle 80.

Thereafter, the surgeon secures the appropriately sized stemless humeralcomponent 10 (i.e., a component 10 having a diameter selected throughtrialing as described above) to the implant insertion tool 330. Thesurgeon first positions the locking collar 362 of the implant insertiontool 330 in an unlocked or release position in which the cam followers354 of implant insertion tool's locking arms 352 are positioned near theinner end 370 of the locking collar's cam surface 368 therebypositioning the locking pawls 356 at their greatest distance away fromone another. The surgeon then positions the insertion tool's alignmentflange 346 in engagement with the stemless humeral component 10 suchthat its alignment pin 350 and alignment keys 348 are positioned in thestemless humeral component's tapered bore 40 and viewing windows 30,respectively. Doing so positions the locking pawls 356 of the implantinsertion tool's locking arms 352 in the stemless humeral component'sremaining viewing windows 30 (i.e., the viewing windows 30 not occupiedby the alignment keys 348).

The surgeon rotates the locking collar 362 clockwise to move the lockingcollar 362 from its unlocked position to its locked position. Suchrotation of the locking collar 362 causes each of the cam followers 354of the implant insertion tool's locking arms 352 to ride along itscorresponding cam surfaces 368 in the direction from its inner end 370to its outer end 372. Doing so causes the cam followers 354 to move inthe direction away from one another thereby causing the locking arms 352to pivot such that the locking pawls 356 are moved in a direction towardone another. Such movement of the locking pawls 356 in the directiontoward one another causes the locking pawls 356 to engage the lips 74 ofthe undercuts 70 formed in the bottom surface 18 of the stemless humeralcomponent's support flange 14 thereby securing the stemless humeralcomponent 10 to the implant insertion tool 330.

Thereafter, as shown in FIG. 33, the surgeon uses the impaction handle80 to position the stemless humeral component 10 such that each of itslegs 16 is aligned with, and inserted into, one of the punched holes 416formed in the patient's surgically-resected humeral surface 414. Doingso also aligns the elongated sleeve 36 of the stemless humeral component10 with the divot 418/drilled hole 422 formed in the patient'ssurgically-resected humeral surface 414 (or the drilled center).

Once the stemless humeral component 10 is positioned in the punchedholes 416 and the divot 418/drilled hole 422 in such a manner, thesurgeon strikes the metal plate 90 of the impaction handle 80 with asurgical mallet, sledge, or other impaction tool to drive the stemlesshumeral component 10 into the bone tissue until the stemless humeralcomponent 10 is fully seated on the patient's planar surgically-resectedhumeral surface 414. The surgeon may use the viewing windows 30 tovisualize the surgically-resected humeral surface 414 to ensure thestemless humeral component 10 is fully seated thereon.

The surgeon then releases the stemless humeral component 10 from theimplant insertion tool 330. To do so, the surgeon rotates the lockingcollar 362 of the implant insertion tool 330 counterclockwise from itslocked position to its unlocked position. Such rotation of the lockingcollar 362 causes each of the cam followers 354 of the implant insertiontool's locking arms 352 to ride along its corresponding cam surfaces 368in the direction from its outer end 372 to its inner end 370. Doing socauses the cam followers 354 to move in the direction toward one anotherthereby causing the locking arms 352 to pivot such that the lockingpawls 356 are moved in a direction away from one another. Such movementof the locking pawls 356 in the direction away from one another causesthe locking pawls 356 to release the lips 74 of the undercuts 70 formedin the bottom surface 18 of the stemless humeral component's supportflange 14 thereby releasing the stemless humeral component 10 from theimplant insertion tool 330. As shown in FIG. 34, the surgeon then liftsthe impaction handle 80, and hence the implant insertion tool 330, awaythereby exposing the implanted stemless humeral component 10.

Once the stemless humeral component 10 has been implanted on thesurgically resected surface 414 of the humerus 400, the surgeon may thenperform a trial of the fit of the final humeral head component 12. To doso, the surgeon installs an appropriately sized trial head component 210(i.e., the size selected during the earlier trialing steps) to theimplanted stemless humeral component 10. The surgeon installs the trialhead component 210 on implanted stemless humeral component 10 byinserting its center lug 218 (see FIGS. 12 and 13) into the tapered bore40 of the implanted stemless humeral component 10 and thereafterpressing or otherwise urging the trial head component 210 downwardlyuntil it fully seats on the implanted stemless humeral component 10. Thecenter lug's annular bands 222 frictionally engage the sidewalls of thetapered bore 40 to frictionally secure the center lug, and hence thetrial head component 210, to the implanted stemless humeral component10. The surgeon then utilizes the trial head component 210 to assesscoverage, soft tissue tension, and range of motion.

Once the surgeon is satisfied, the trial head component 210 is thenremoved and replaced with the ultimate humeral head component 12. Inparticular, as shown in FIG. 35, the surgeon then installs anappropriately sized humeral head component 12 (i.e., the size selectedduring the earlier trialing steps) to the implanted stemless humeralcomponent 10. The surgeon installs the humeral head component 12 onimplanted stemless humeral component 10 by inserting its tapered post 42into the tapered bore 40 of the stemless humeral component's elongatedsleeve 36 (see FIG. 36).

The head impaction tool 380 may be used to impact, and hence taper lock,the head component 12 to the stemless humeral component 10. To do so, asshown in FIG. 35, the surgeon first secures the head impaction tool 380to the impaction handle 80 by inserting the handle's D-shaped connectingpin 104 into the round opening 386 of the head impaction tool'sconnector 384 until one of the connector's lip 392 is engaged by thelocking pawl 102 of the impaction handle's attachment mechanism 86 (seeFIGS. 6 and 7) to secure the head impaction tool 380 to the impactionhandle 80.

The surgeon then positions the impaction handle 80 that the headimpaction tool's concave impact surface 396 is placed in contact withthe generally hemispherically-shaped outer surface of the head component12. The surgeon then strikes the impact handle's metal strike plate 90with a surgical mallet, sledge, or other impaction tool to drive thehumeral head component 12 downwardly so as to urge the tapered post 42of the humeral head component 12 into contact with the sidewall definingthe tapered bore 40 of the elongated sleeve 36 thereby taper locking thehumeral head component 12 to the stemless humeral component 10. Suchfinal assembly of the humeral head component 12 to the stemless humeralcomponent 10 is shown in FIG. 36.

Referring now to FIG. 37, there is shown another embodiment of animplant insertion tool 540 that may be secured to the stemless humeralcomponent 10 to facilitate implantation of the stemless humeralcomponent 10 into the patient's surgically-prepared humeral surface 414.The implant insertion tool 540 includes a body 542 having an elongatedbore 544 extending therethrough. A locking rod 548 is captured in thebore 544. In such an arrangement, the locking rod 548 rotates freelywithin the bore 544.

A knob 550 is secured to the proximal end of the locking rod 548. Inaddition to being used to secure the implant insertion tool 540 to thestemless humeral component 10, the knob 550 is also used as an impactsurface. Namely, the surgeon strikes the upper surface 552 of the knob550 to drive the stemless humeral component 10 into the bone tissue ofthe patient's surgically-prepared humeral surface 414.

The locking rod 548 has a set of locking threads 556 formed in itsdistal end (i.e., the end opposite the knob 550). The threads 556 aresized to be received into the complimentary threads 50 of the threadedbore 48 formed in the elongated sleeve 36 of the stemless humeralcomponent 10. When a surgeon or other user rotates the knob 550, thelocking screw's threads 556 are likewise rotated. Rotation in onedirection (e.g., clockwise) may be used to tighten, and hence secure,the implant insertion tool 540 to the stemless humeral component 10,with rotation in the opposite direction (e.g., counterclockwise) beingused to loosen, and hence, uncouple the implant insertion tool 540 fromthe stemless humeral component 10.

As can be seen in FIG. 37, a number of straight flutes or ridges 558 areformed in the end of the of the implant insertion tool's body 542 nearthe knob 550 of the locking rod 548. The ridges 558 function as a gripfor allowing the surgeon to hold the implant insertion tool 540 duringimplantation of the stemless humeral component 10.

The end of the of the implant insertion tool's body 542 near the threads556 of the locking rod 548 has an alignment collar 560 formed therein.The alignment collar 560 is embodied as an annular flange extendingoutwardly from the longitudinal axis of implant insertion tool's body542. The alignment collar 560 has a number of protrusions or alignmentkeys 562 extending downwardly from its lower surface 564. As can be seenin FIG. 37, the alignment keys 562 are sized, shaped, and positioned tobe received into the viewing windows 30 formed in the stemless humeralcomponent 10. With the alignment keys 562 positioned in the viewingwindows 30, the stemless humeral component 10 is prevented from rotatingrelative the implant insertion tool 540 during rotation of the implantinsertion tool's knob 550 thereby allowing the implant insertion tool'sthreads 556 to engage (or disengage) the stemless humeral component'sthreads 50.

In a manner similar to as described above in FIG. 33, the surgeonsecures the stemless humeral implant 10 to the implant insertion tool540 then uses the implant insertion tool 540 to align the stemlesshumeral component's legs 16 and elongated sleeve 36 to the punched holes416 and the divot 418/drilled hole 422, respectively, formed in thesurgically-resected humeral surface 414. Once the stemless humeralcomponent 10 is positioned in the punched holes 416 and the divot418/drilled hole 422 in such a manner, the surgeon strikes the uppersurface 552 of the knob 550 with a surgical mallet, sledge, or otherimpaction tool to drive the stemless humeral component 10 into the bonetissue until the stemless humeral component 10 is fully seated on thepatient's planar surgically-resected humeral surface 414. The surgeonmay use the viewing windows 30 to visualize the surgically-resectedhumeral surface 414 to ensure the stemless humeral component 10 is fullyseated thereon.

The components of the implant insertion tool 540 (i.e., its body 542 andthe locking rod 548) may be constructed from a medical-grade metal suchas stainless steel, cobalt chrome, or titanium, although other metals oralloys may be used. Moreover, in some embodiments, rigid polymers suchas polyetheretherketone (PEEK) may also be used.

Referring now to FIG. 38, there is shown another embodiment of animplant insertion tool 580. The implant insertion tool 580 may besecured to the stemless humeral component 10 to facilitate implantationof the stemless humeral component 10 into the patient'ssurgically-prepared humeral surface. The implant insertion tool 580includes a body 582 having an elongated bore 584 extending therethrough.A locking rod such as a locking screw 588 is captured in the bore 584.In such an arrangement, the locking screw 588 rotates freely within thebore 584, but is prevented from being removed from the bore 584 (i.e.,it is not removable from the implant insertion tool's body 582).

A D-shaped drive head 590 is formed in the proximal end of the lockingscrew 588, with a number of locking threads 592 being formed in itsopposite, distal end. The threads 582 are sized to be received into thecomplimentary threads 50 of the threaded bore 48 formed in the elongatedsleeve 36 of the stemless humeral component 10. The D-shaped drive head590 is sized, shaped, and positioned to receive a D-shaped head of aratchet or other surgical tool. As such, when the head of the racket isinserted in the implant insertion tool's drive head 590 and rotated, thelocking screw's threads 592 are likewise rotated. Rotation in onedirection (e.g., clockwise) may be used to tighten, and hence secure,the implant insertion tool 580 to the stemless humeral component 10,with rotation in the opposite direction (e.g., counterclockwise) beingused to loosen, and hence, uncouple the implant insertion tool 580 fromthe stemless humeral component 10.

The end of the of the implant insertion tool's body 582 near the drivehead 590 of the locking screw 588 has a channel 596 formed therein. Thesidewalls of implant insertion tool's body 582 into which the channel596 is formed define an undercut 598 that extends along the length ofthe channel 596. The undercut 598 takes the form of a lip 602 positionedat the top of the channel 596. The lip 602 is engaged by the lockingpawl 102 of the impaction handle's attachment mechanism 86 (see FIGS. 6and 7) to secure the implant insertion tool 580 to the impaction handle80.

In a manner similar to as described above in FIG. 33, the surgeonsecures the implant insertion tool 580 to the impaction handle 80 andthereafter secures the stemless humeral implant 10 to the implantinsertion tool 580 or vice versa. The surgeon then uses the impactionhandle 80 to align the stemless humeral component's legs 16 andelongated sleeve 36 to the punched holes 416 and the divot 418/drilledhole 422 formed in the surgically-resected humeral surface 414. Once thestemless humeral component 10 is positioned in the punched holes 416 andthe divot 418/drilled hole 422 in such a manner, the surgeon strikes themetal plate 90 of the impaction handle 80 with a surgical mallet,sledge, or other impaction tool to drive the stemless humeral component10 into the bone tissue until the stemless humeral component 10 is fullyseated on the patient's planar surgically-resected humeral surface 414.The surgeon may use the viewing windows 30 to visualize thesurgically-resected humeral surface 414 to ensure the stemless humeralcomponent 10 is fully seated thereon.

The components of the implant insertion tool 580 (i.e., its body 582 andthe locking screw 588) may be constructed from a medical-grade metalsuch as stainless steel, cobalt chrome, or titanium, although othermetals or alloys may be used. Moreover, in some embodiments, rigidpolymers such as polyetheretherketone (PEEK) may also be used. In otherembodiments, the implant insertion tool 580 may be formed as a singlemonolithic component. In such embodiments, the implant insertion tool580 may be threaded onto the implant or clipped onto the impactionhandle for threading onto the implant. In other embodiments, the implantinsertion tool 580 may include a connecting collar that surrounds theD-shaped drive socket. As such, the D-shaped drive socket 630 may berotatable relative to the connecting collar.

Referring now to FIGS. 39 and 40, there is shown another embodiment ofan implant insertion tool 620. The implant insertion tool 620 may besecured to the stemless humeral component 10 to facilitate implantationof the stemless humeral component 10 into the patient'ssurgically-prepared humeral surface 414. The implant insertion tool 620includes a somewhat ring-shaped body 622 having an upper bore 624extending through an upper portion of its body 622 and lower bore 626extending through a lower portion of its body 622. The two bores 624,626 are coaxial with one another (i.e., they share a common centralaxis). A locking rod 628 is captured in the bores 624, 626. In such anarrangement, the locking rod 628 rotates freely within the bores 624,626, but is prevented from being removed from the bores 624, 626 (i.e.,it is not removable from the implant insertion tool's body 622).

A D-shaped drive socket 630 is formed in the proximal end of the lockingrod 628, with a number of locking threads 632 being formed in itsopposite, distal end. The threads 632 are sized to be received into thecomplimentary threads 50 of the threaded bore 48 formed in the elongatedsleeve 36 of the stemless humeral component 10 (see FIG. 5). TheD-shaped drive socket 630 is sized, shaped, and positioned to receivethe D-shaped connecting pin 104 of the attachment mechanism 86 of theimpaction handle 80 (see FIG. 6).

As can be seen in FIGS. 39 and 40, the ring-shaped body 622 of theimplant insertion tool 620 includes a connecting collar 634 thatsurrounds the D-shaped drive socket 630 of the locking rod 628. As such,the D-shaped drive socket 630 of the locking rod 628 is rotatablerelative to the connecting collar 634 of the implant insertion tool'sring-shaped body 622. The outer surface of the connecting collar 634 hasa number of ratchet slots 636 formed therein. One end 638 of the ratchetslots 636 is wider than its other end 640 thereby giving the ratchetsslots 636 a generally L-shaped configuration. The sidewall 642 definingthe narrow end 640 of the ratchet slots 636 defines a ramped-shaped orotherwise angled cam surface 644, whereas the sidewall 646 defining thewide end 638 of the ratchet slots 636 defines a vertical stop surface648. When the impaction handle's connecting pin 104 is inserted in theimplant insertion tool's D-shaped drive socket 630, the locking pawl 102of the impaction handle's attachment mechanism 86 (see FIGS. 6 and 7) ispositioned in one of the ratchet slots 636. The configuration of theratchet slots 636 permits rotation of the impaction handle 80 (and hencethe locking rod 628) relative to the ring-shaped body 622 of the implantinsertion tool 620 in one direction (e.g., clockwise), but preventsrotation in the opposite direction (e.g., counterclockwise). Inparticular, rotation of the impaction handle 80 (and hence the lockingrod 628) relative to the ring-shaped body 622 in the clockwise directioncauses the leading edge of the locking pawl 102 of the impactionhandle's attachment mechanism 86 (see FIGS. 6 and 7) to contact theramped-shaped cam surface 644 that defines the narrow end 640 of theratchet slot 636 in which the locking pawl 102 is captured. Continuedclockwise rotation causes the locking pawl 102 to ride up theramped-shaped cam surface 644 (as the spring bias of the springimpaction handle's 110 is overcome) and out of the ratchet slot 636. Thelocking pawl 102 rides on the outer surface of the connecting collar 634between two adjacent ratchet slots 636 until the trailing edge of thelocking pawl 102 clears the vertical stop surface 648 of the ratchetslot 636 adjacent to the one just exited by the locking pawl 102 atwhich point the spring bias of the spring impaction handle's 110 urgesthe locking pawl 102 downwardly into the ratchet slot 636.

Conversely, rotation of the impaction handle 80 (and hence the lockingrod 628) relative to the ring-shaped body 622 in the counterclockwisedirection causes the leading edge of the locking pawl 102 of theimpaction handle's attachment mechanism 86 (see FIGS. 6 and 7) tocontact the vertical stop surface 648 of the ratchet slot 636 thatdefines the wide end 638 of the ratchet slot 636 in which the lockingpawl 102 is captured. Such contact with the vertical stop surface 648prevents further rotation of the impaction handle 80 (and hence thelocking rod 628) relative to the ring-shaped body 622 in thecounterclockwise direction.

Such ratchet-type clockwise rotation of the impaction handle 80 (andhence the locking rod 628) relative to the ring-shaped body 622 is usedto secure the stemless humeral component 10 to the implant insertiontool 620. In particular, when the impaction handle 80 is installed onthe implant insertion tool 620 and rotated, the locking rod's threads632 are likewise rotated. Rotation in one direction (e.g., clockwise)may be used to tighten, and hence secure, the implant insertion tool 580to the stemless humeral component 10. Rotation in the opposite direction(e.g., counterclockwise) is used to loosen, and hence, uncouple theimplant insertion tool 620 from the stemless humeral component 10. Inorder to perform such counterclockwise rotation, the surgeon presses andholds down on the actuation arm 98 of the impaction handle's lever 94thereby lifting the impaction handle's locking pawl 102 out of theratchets slots 636 of the implant insertion tool 620.

The end of the of the implant insertion tool's ring-shaped body 622 nearthe threads 632 of the locking rod 628 has an alignment collar 652formed therein. The alignment collar 652 is embodied as an annularflange formed in the distal end 654 of the implant insertion tool's body622. The alignment collar 652 has a number of protrusions or alignmentkeys 656 extending downwardly from its lower surface 658. As can be seenin FIG. 40, the alignment keys 656 are sized, shaped, and positioned tobe received into the viewing windows 30 formed in the stemless humeralcomponent 10. With the alignment keys 656 positioned in the viewingwindows 30, the stemless humeral component 10 is prevented from rotatingrelative the implant insertion tool 620 during rotation of the implantinsertion tool's locking rod 628 thereby allowing the implant insertiontool's threads 632 to engage (or disengage) the stemless humeralcomponent's threads 50.

In a manner similar to as described above in FIG. 33, the surgeonsecures the implant insertion tool 620 to the impaction handle 80 andthereafter secures the stemless humeral implant 10 to the implantinsertion tool 620. The surgeon then uses the impaction handle 80 toalign the stemless humeral component's legs 16 and elongated sleeve 36to the punched holes 416 and the divot 418/drilled hole 422 formed inthe surgically-resected humeral surface 414. Once the stemless humeralcomponent 10 is positioned in the punched holes 416 and the divot 418 insuch a manner, the surgeon strikes the metal plate 90 of the impactionhandle 80 with a surgical mallet, sledge, or other impaction tool todrive the stemless humeral component 10 into the bone tissue until thestemless humeral component 10 is fully seated on the patient's planarsurgically-resected humeral surface 414. The surgeon may use the viewingwindows 30 to visualize the surgically-resected humeral surface 414 toensure the stemless humeral component 10 is fully seated thereon.

The components of the implant insertion tool 620 (i.e., its body 622 andthe locking rod 628) may be constructed from a medical-grade metal suchas stainless steel, cobalt chrome, or titanium, although other metals oralloys may be used. Moreover, in some embodiments, rigid polymers suchas polyetheretherketone (PEEK) may also be used.

Referring now to FIGS. 41 and 42, there is shown another embodiment ofan head resection guide 670 that may be used as a cutting guide to guidethe advancement of a bone saw blade to resect the humeral head of thepatient. Unlike the head resection guide 290 described above in regardto FIGS. 17-19, the head resection guide 670 is not adjustable, butrather is provided in a number of varying sizes (i.e., varyingdiameters) to fit the needs of a given patient. The head resection guide670 includes a generally rectangular-shaped base 672 having acircular-shaped ring 674 secured thereto. The ring 674 extends outwardlyfrom the base 672 and defines a circular-shaped opening 676. As will bedescribed in more detail below, the patient's humeral head is capturedin the opening 676 during resection thereof.

The head resection guide 670 has a connector 678 that may be engaged bythe attachment mechanism 126 of the alignment handle 120 to secure thehead resection guide 670 to the alignment handle 120. The connector 678has a key-hole shaped opening 680 formed therein. The key-hole opening680 is sized and shaped to receive the keying pin 144 formed in thedistal end of the alignment handle's body 122. The connector 678 alsohas a channel 682 formed therein. An undercut 684 is formed along thelength of the channel 682. The undercut 684 takes the form of a lip 686positioned at the top of the channel 682 and extending outwardly intothe channel 682. The lip 686 is engaged by the locking pawl 142 of thealignment handle's attachment mechanism 126 (see FIGS. 8 and 9) tosecure the head resection guide 670 to the alignment handle 120.

The head resection guide's base 672 has a number of pin holes 692 formedtherein. As will be discussed in more detail, surgical pins may beinserted through the pin holes 692 to pin the head resection guide 670to the patient's humerus during resection of the patient's naturalhumeral head.

As can be seen in FIG. 42, both the base 672 and the ring 674 includeplanar surfaces that cooperate to define a cutting guide surface forguiding a bone saw blade to resect the patient's natural humeral head.Specifically, the base 672 includes a planar anterior guide surface 694that aligns in a coplanar relationship with a planar posterior guidesurface 696 of the ring 674. As described above, in the illustrativeembodiment described herein, the head resection guide 670 is embodied asa monolithic structure. Hence, the two guide surfaces 694, 696 areembodied as a common surface that collectively defines a cutting surfaceupon which a bone saw blade may be supported (i.e., guided) during acutting operation to resect the patient's natural humeral head.

In use, the surgeon installs the head resection guide 670 to thealignment handle 120 by inserting the keying pin 144 formed in thedistal end of the alignment handle's body 122 into the key-hole opening680 of the head resection guide's connector 678. In doing so, theconnector's lip 686 is engaged by the locking pawl 142 of the alignmenthandle's attachment mechanism 126 (see FIGS. 8 and 9) thereby securingthe head resection guide 670 to the alignment handle 120.

In a similar manner to as described above in regard to FIG. 26, thesurgeon then uses the head resection guide 670 as a cutting guide tofacilitate the surgical resection of the patient's humeral head 402. Todo so, the surgeon uses the alignment handle 120 to position the headresection guide 670 around the patient's humeral head 402 such that theposterior section 702 of the ring 674 rests on the posterior cuffinsertion site of the patient's rotator cuff. Doing so protects theposterior rotator cuff during head resection and acts as a step inplacing the guide at the correct height and version. The surgeon thenpositions the anterior guide surface 694 of the base 672 relative to theanterior surface 404 of the patient's humerus 400 at the desiredresection angle and height. The surgeon may then make any necessaryminor adjustments to the positions of the anterior surface of the baserelative to the anterior surface 404 and the anterior guide surface 694relative to the articular margin to finalize the desired resection angleand height. Thereafter, the surgeon may insert a surgical pin 406 (seeFIG. 26) through each of the pin holes 692 to pin the head resectionguide 670 to the patient's humerus 400 to maintain the anterior guidesurface 694 in its desired position. Once pinned in place, the surgeondisconnects the alignment handle 120 from the head resection guide 670.

Similar to as described in regard to FIG. 26, the surgeon then operatesa bone saw, such as an oscillating power saw 408, to resect thepatient's humeral head 402. To do so, the surgeon positions the sawblade 410 of the power saw 408 on the planar anterior guide surface 694of the head resection guide's base 672. The surgeon then actuates theoscillating power saw 408 and applies pressure on it so that it advancesposteriorly and into contact with the anterior surface 404 of thepatient's humerus 400. As the saw blade 410 is advanced posteriorly intocontact with the anterior surface 404 of the humerus 400 and thereafterthrough its midsection in the direction toward its posterior surface412, the oscillating motion of the bone saw 408 abrades the bone tissueof the humeral head 402.

The surgeon continues to posteriorly advance the power saw 408 until thesaw blade 410 exits the bone. Specifically, the surgeon continues tooperate the bone saw 408 until the distal end of its blade 410 passesbeyond the posterior surface 412 of the humeral head 402. Upon exit fromthe posterior surface 412 of the bone, the saw blade 410 is supportedand guided by the posterior guide surface 696 of the ring 674. In such away, the posterior guide surface 696 of the ring 674 prevents the sawblade 410 from contacting the patient's posterior rotator cuff. Once thesaw blade 410 has exited the bone and advanced onto the posterior guidesurface 696 of the ring 674, the surgeon may deactuate the bone saw 408and thereafter then lift away the resected portion of the patient'shumeral head 402.

The head resection guide 670 may be constructed from a medical-grademetal such as stainless steel, cobalt chrome, or titanium, althoughother metals or alloys may be used. Moreover, in some embodiments, rigidpolymers such as polyetheretherketone (PEEK) may also be used.

Referring now to FIGS. 43 and 44, there is shown another embodiment ofthe stemless humeral component 10. The features of the embodimentillustrated in FIGS. 43 and 44 are substantially similar to thosediscussed above in reference to the embodiment of FIGS. 1-5. Suchfeatures are designated in FIGS. 43 and 44 with the same referencenumbers as those used in FIGS. 1-5. In essence, the embodiment of FIGS.43 and 44 is substantially the same as the embodiment of FIGS. 1-5 witha few exceptions. For example, the suture holes 26 have been removedfrom the stemless humeral component of FIGS. 43 and 44. In such a case,the surgeon may use the viewing windows 30 in lieu of the removed sutureholes 26 to suture bone wafers or soft tissue to the stemless humeralcomponent 10. To accommodate such use of the viewing windows 30, theedges of the stemless humeral component's support flange 14 defining theviewing windows 30 may be rounded.

Referring now to FIGS. 45 and 46, there is shown another embodiment ofthe sizing instrument 160. The features of the embodiment illustrated inFIGS. 45 and 46 are substantially similar to those discussed above inreference to the embodiment of FIGS. 10 and 11. Such features aredesignated in FIGS. 45 and 46 with the same reference numbers as thoseused in FIGS. 10 and 11. In essence, the embodiment of FIGS. 45 and 46is substantially the same as the embodiment of FIGS. 10 and 11 with afew exceptions. For example, the viewing windows 180 have been removedfrom the sizing instrument 160 of FIGS. 45 and 46.

Moreover, the geometry of the punch guide holes 170 has been altered. Inparticular, the punch guide holes 170 are substantially T-shaped in theembodiment of the sizing instrument 160 shown in FIGS. 45 and 46. Insuch a way, the geometry of the punch guide holes 170 more closelycorresponds with the geometry of the T-shaped tines 252 of the surgicalpunch 240.

In addition, the geometry of the connector 182 has been altered in theembodiment of the sizing instrument 160 shown in FIGS. 45 and 46. Toaccommodate such a change, the attachment mechanism 126 of the alignmenthandle 120 may also be altered to secure the sizing instrument 160thereto.

Referring now to FIG. 47, there is shown another embodiment of thesurgical punch 240. The features of the embodiment illustrated in FIG.47 are substantially similar to those discussed above in reference tothe embodiment of FIG. 14. Such features are designated in FIG. 47 withthe same reference numbers as those used in FIG. 14. In essence, theembodiment of FIG. 47 is substantially the same as the embodiment ofFIG. 14 with a few exceptions. For example, the center spike 262 hasbeen removed from the surgical punch 240 of FIG. 47. In such a case, thesurgeon may use the center drill 270 to drill a hole in the patient'ssurgically-prepared humerus to accommodate the elongated sleeve 36 ofthe stemless humeral component 10 in the manner discussed above.

Moreover, the struts 268 have been removed such that the tines 252 aremore integrally formed in the surgical punch's body 242. In addition,the geometry of the surgical punch's connecting socket 260 andconnecting channel 246 have been altered in the embodiment of thesurgical punch 240 shown in FIG. 47. To accommodate such a change, theattachment mechanism 86 of the impact handle 80 may also be altered tosecure the surgical punch 240 thereto.

Moreover, as can be seen in FIG. 47, the proximal end 266 of each of theribs 256 of the tines 252 (i.e., the end secured to the punch's shaft244) is wider than the opposite, distal end 288 of each rib 256. Assuch, the corresponding shape of the punched holes formed in thepatient's surgically-prepared humerus is wider at its open end than atits blind end. Such a widened opening facilitates insertion of thecantilevered legs 16 of the stemless humeral component 10.

Referring now to FIG. 48, there is shown another embodiment of theimplant insertion tool 540. The features of the embodiment illustratedin FIG. 48 are substantially similar to those discussed above inreference to the embodiment of FIG. 37. Such features are designated inFIG. 48 with the same reference numbers as those used in FIG. 37. Inessence, the embodiment of FIG. 48 is substantially the same as theembodiment of FIG. 37 with a few exceptions. For example, the size ofthe knob 552 is larger in the embodiment of FIG. 48 to facilitate usethereof by the surgeon. Moreover, the implant insertion tool's grip isovermolded to the tool's body 542.

Referring now to FIGS. 49-52, there is shown a drill guide 710 that maybe used to pre-drill the patient's surgically-prepared humeral surfaceprior to implantation of the stemless humeral component 10. In such acase, the surgeon may opt to subsequently punch the patient'ssurgically-prepared humeral surface prior to implantation of thestemless humeral component 10 in the manner described above (i.e., usethe surgical punch 240 after such pre-drilling). Alternatively, thesurgeon may drill the patient's surgically-prepared humeral surface inlieu of the punch procedure.

As described above, the stemless humeral component 10 may be provided invarious sizes (i.e., diameters) to fit the needs of a given patient. Forexample, the stemless humeral component 10 may be provided in ninedifferent sizes. Each of such differently-sized components 10 has legsof different thicknesses and lengths. As such, if discrete drill guidesare used for each differently-sized stemless humeral component 10,multiple differently-sized drill guides would be required (e.g., ninedifferently sized drill guides would be required for ninedifferently-sized stemless humeral components 10). Moreover, to avoidoverly thick drill guides for the smaller sizes of stemless humeralcomponents 10, multiple different drill sizes may be required. As willbe discussed below in more detail, the drill guide 710 avoids the needfor such differently-sized drill guides and drills.

The drill guide 710 includes a body 712 having a generally planar lowersurface 714, and an opposite, stepped upper surface 716. As can be seenin FIG. 49, the stepped upper surface 716 is spiral shaped and, beingstepped, includes a plurality of discrete generally planar drill-stopsurfaces 718. Each of the drill-stop surfaces 718 is spaced apart fromthe lower surface 714 of the drill guide's body 712 by a differentlength. As a result, the drill guide's body 712 has a differentthickness at the locations corresponding to each of the differentdrill-stop surfaces 718.

As can be seen in FIGS. 49 and 50, each of the drill-stop surfaces 718has a number of guide bores 730 formed therein. The guide bores 730 areconfigured to guide the peripheral drill bit 272 during drilling of thepatient's surgically-prepared humeral surface. As such each of the guidebores 730 extends throughout the entire thickness of the guide body 712.In other words, one end of each of the guide bores 730 opens into thedrill-stop surface 718, with the other end opening into the lowersurface 714. As described above, the collar 284 of the peripheral drillbit 272 functions as a depth stop to ensure the drill bit 272 drillssurgically-prepared holes at a desired depth. As such, the peripheraldrill bit 272 may be advanced through one of the guide bores 730 andinto the bone tissue until the lower surface 286 of the collar 284bottoms out or otherwise engages the selected drill-stop surface 718.

Each of the drill-stop surfaces 718 corresponds to a differently-sizedstemless humeral component 10. For example, a drill-stop surface 720 atthe “bottom” end 722 of the spiral-shaped stepped upper surface 716corresponds to the largest size of stemless humeral component 10, withthe a drill-stop surface 724 at the “top” end 726 of the spiral-shapedstepped upper surface 716 corresponding to the smallest size of stemlesshumeral component 10. The remaining drill-stop surfaces 718 correspondto the remaining sizes of the stemless humeral component 10 with thesize of the corresponding component 10 increasing along the steppedupper surface 716 in the direction from its top end 726 to its bottomend 722.

Because each of the drill-stop surfaces 718 is spaced apart from thelower surface 714 of the drill guide's body 712 by a different length,the peripheral drill bit 272 will drill to different depths of thepatient's surgically-prepared humeral surface depending on whichdrill-stop surface 718 is used by the surgeon. For example, if thesurgeon utilizes the guide holes 730 of the drill-stop surface 724 atthe “top” end 726 of the spiral-shaped stepped upper surface 716,shallower drilled holes will be produced than if the surgeon utilizesthe guide bores 730 of the drill-stop surface 720 at the “bottom” end722 of the spiral-shaped stepped upper surface 716 since the collar 284of the drill bit 272 will bottom out on the drill-stop surface 724 priorto when it will bottom out on the lower-positioned drill-stop surface720. As such, the drill bit 272 will progressively drill deeper at thedrill-stop surfaces 718 along stepped upper surface 716 in the directionfrom its top end 726 to its bottom end 722.

As can be seen in FIGS. 50 and 51, the guide bores 730 of each of thedrill-stop surfaces 718 are arranged in a unique hole pattern relativeto the remaining drill-stop surfaces 718. For example, the drill-stopsurface 720 at the “bottom” end 722 of the spiral-shaped stepped uppersurface 716 corresponding to the largest size of stemless humeralcomponent 10 has a relatively large hole pattern (i.e., the guide bores730 are more spread out relative to the other hole patterns), whereasthe drill-stop surface 724 at the “top” end 726 of the spiral-shapedstepped upper surface 716 corresponding to the smallest size of stemlesshumeral component 10 has a relatively small hole pattern (i.e., theguide bores 730 are more compact relative to the other hole patterns).In such a way, the hole pattern corresponds to the size of thecantilevered legs 16 of the differently-sized stemless humeralcomponents 10, with larger hole patterns corresponding to largercomponent legs 16 and smaller hole patterns corresponding to smallercomponent legs 16. That is, the drill-stop surfaces 718 correspond tothe sizes of the stemless humeral component 10 with the size of thecorresponding component 10 increasing along the stepped upper surface716 in the direction from its top end 726 to its bottom end 722.

As can be seen in FIGS. 49 and 51, the guide body 712 has an elongatedboss 732 secured to, and extending downwardly from, its lower surface714. The elongated boss 732 is configured to be received into theelongated bore 168 of the sizing instrument 160 to secure the drillguide 710 thereto. An elongated grip 734 is secured to, and extendsupwardly from, the stepped upper surface 716. The grip 734 has a numberof grooves 736 formed therein and is used by the surgeon to grasp thedrill guide 710.

As shown in FIG. 51, the guide body 712 has a number of alignment keys738 formed in its lower surface 714. The alignment keys 738 are receivedinto a number of alignment slots 740 formed in the sidewall of thesizing instrument's elongated bore 168 (see FIG. 52) to correlate theproper drill-stop surface 718 with the correct size of the sizinginstrument 160. In particular, the alignment slots 740 of each of thedifferently-sized sizing instruments 160 are placed in annular locationsunique to the particular sizing instrument 160 (i.e., each of thedifferently-sized sizing instruments has a unique slot configuration).When the alignment keys 738 of the drill guide 710 are advanced into theuniquely-positioned alignment slots 740, the proper drill-stop surface718 corresponding to the particular size of the sizing instrument 160will be positioned over one of the sizing instrument's guide punch holes170 thereby “keying” the stepped upper surface 716 of the drill guide710 to the particular size of the sizing instrument 160.

Like other of the instruments described herein, the drill guide 710 maybe constructed with a biocompatible metal such as stainless steel,cobalt chrome, or titanium, although other metals or alloys may be used.The drill guide 710 may also be embodied as a polymer instrument. Assuch, drill guide 710 may be made of any suitable medical-gradepolymeric material such as polyetheretherketone (PEEK). In such anembodiment, the polymer drill guide 710 may include metallic inserts(e.g., sleeves) positioned in the drill guide bores 730.

In operation, the surgeon may use the drill guide 710 to drill a numberof holes in the patient's surgically-prepared humeral surface. To do so,the surgeon first selects a size of the stemless humeral component 10 toimplant in the patient's humerus in the manner described above. Such aselection may be performed preoperatively or as a result ofintra-operative changes based on use of the sizing instrument 160. Thesurgeon then secures a sizing instrument 160 that corresponds to theselected size of the stemless humeral component 10 to thesurgically-prepared surface of the patient's humerus in the mannerdescribed above in regard to FIG. 27.

The surgeon then selects a drill-stop surface 718 of the drill guide 710that corresponds to the selected size of the stemless humeral component10 from the plurality of drill-stop surfaces 718 formed in the drillguide's stepped upper surface 716. The surgeon may then attach the drillguide 710 to the sizing instrument 160 by advancing the drill guide'selongated boss 732 into the elongated bore 168 of the sizing instrument160. During such advancement, the alignment keys 738 of the drill guide710 are advanced into the uniquely-positioned alignment slots 740 of thesizing instrument 160 thereby causing the drill-stop surface 718corresponding to the particular size of the selected sizing instrument160 to be positioned over one of the sizing instrument's guide punchholes 170.

The surgeon may then advance the peripheral drill 272 through each ofthe guide bores 730 of the selected drill-stop surface 718 and into thebone tissue until the drill's collar 284 bottoms out or otherwiseengages the selected drill-stop surface 718. The surgeon may then rotatethe drill guide 710 such that the selected drill-stop surface 718 ispositioned over a different one of the remaining punch guide holes 170of the sizing instrument 160. Thereafter, the surgeon advances theperipheral drill 272 through each of the guide bores 730 and repeats theprocess at each of the remaining punch guide holes 170.

The surgeon may then utilize the surgical punch 240 in a similar mannerto as described above in regard to FIG. 29 to punch the now pre-drilledsurgically-prepared surface of the patient's humerus and thereafterimplant the stemless humeral component 10 in a similar manner to asdescribed above in regard to FIG. 33. Alternatively, the surgeon mayimplant the stemless humeral component 10 into the drilledsurgically-prepared surface of the patient's humerus without firstutilizing the surgical punch 240.

While the disclosure has been illustrated and described in detail in thedrawings and foregoing description, such an illustration and descriptionis to be considered as exemplary and not restrictive in character, itbeing understood that only illustrative embodiments have been shown anddescribed and that all changes and modifications that come within thespirit of the disclosure are desired to be protected.

There are a plurality of advantages of the present disclosure arisingfrom the various features of the apparatus, system, and method describedherein. It will be noted that alternative embodiments of the apparatus,system, and method of the present disclosure may not include all of thefeatures described yet still benefit from at least some of theadvantages of such features. Those of ordinary skill in the art mayreadily devise their own implementations of the apparatus, system, andmethod that incorporate one or more of the features of the presentinvention and fall within the spirit and scope of the presentdisclosure.

1-23. (canceled)
 24. A surgical instrument assembly for use during asurgical procedure to implant a stemless humeral component to replacethe humeral head of a patient's humerus, comprising: a sizing instrumenthaving a size that mimics the size of the stemless humeral component tobe implanted to replace the humeral head of the patient's humerus, thesizing instrument having a generally round body with a plurality ofpunch guide holes formed therein, wherein (i) the round body of thesizing instrument is sized such that the radial outer edge thereof ispositioned in contact with cortical bone tissue of the patient's humeruswhen the sizing instrument is secured to the patient's humerus, and (ii)each of the plurality of punch guide holes is positioned in a locationthat (a) is located over cancellous bone tissue of the patient's humeruswhen the sizing instrument is secured to the patient's humerus, and (b)aligns with a plurality of legs of the stemless humeral component. 25.The surgical instrument assembly of claim 24, wherein: the sizinginstrument has an upper surface and a lower surface, each of the punchguide holes extends from the upper surface to the lower surface, thesizing instrument further includes a number of bone-engaging spikesextending downwardly from its lower surface, and each of the number ofbone-engaging spikes is positioned in a location to engage cancellousbone tissue of the patient's humerus when the sizing instrument issecured to the patient's humerus.
 26. The surgical instrument assemblyof claim 24, wherein each of the punch guide holes of the sizinginstrument is generally T-shaped.
 27. The surgical instrument assemblyof claim 24, wherein: the round body of the sizing instrument isgenerally dome-shaped having a flattened upper surface and a planaropposite, lower surface, an elongated drill guide bore extends through acenter of the sizing instrument from the upper surface to the lowersurface, and the drill guide bore is positioned in a location that islocated over cancellous bone tissue of the patient's humerus when thesizing instrument is secured to the patient's humerus.
 28. The surgicalinstrument assembly of claim 24, further comprising a surgical punchconfigured to punch holes in the cancellous bone tissue of the patient'shumerus to receive the plurality of legs of the stemless humeralcomponent, wherein: the surgical punch comprises a plurality of tines,and each of the plurality of tines of the surgical punch is positionedin a location that aligns with one of the punch guide holes of thesizing instrument.
 29. The surgical instrument assembly of claim 24,further comprising a trial head component, wherein: the trial headcomponent comprises (i) a generally hemispherically-shaped trial bearingsurface, and (ii) an underside surface opposite the trial bearingsurface, and the diameter of the underside surface of the trial headcomponent is substantially the same as the diameter of the round body ofthe sizing instrument.
 30. The surgical instrument assembly of claim 29,wherein: the trial head component further comprises a center lugextending laterally away from the underside surface, and the center lugis configured to be frictionally secured to the sizing instrument whenthe center lug is inserted into an elongated drill guide bore extendingthrough a center of the sizing instrument.
 31. A surgical instrumentassembly for use during a surgical procedure to implant a stemlesshumeral component and a humeral head component to replace the humeralhead of a patient's humerus, comprising: a trial head component having asize that mimics the size of the humeral head component to be implantedin the patient's humerus, the trial head component comprising (i) agenerally hemispherically-shaped trial bearing surface, and (ii) anunderside surface opposite the trial bearing surface, and a sizinginstrument having a size that mimics the size of the stemless humeralcomponent to be implanted in the patient's humerus, the sizinginstrument having a generally round body with a plurality of punch guideholes formed therein, wherein (i) the diameter of the underside surfaceof the trial head component is substantially the same as the diameter ofthe round body of the sizing instrument, and (ii) each of the pluralityof punch guide holes is positioned in a location that aligns with aplurality of legs of the stemless humeral component.
 32. The surgicalinstrument assembly of claim 31, wherein the round body of the sizinginstrument is sized such that the radial outer edge thereof ispositioned in contact with cortical bone tissue of the patient's humeruswhen the sizing instrument is secured to the patient's humerus.
 33. Thesurgical instrument assembly of claim 31, wherein each of the pluralityof punch guide holes is positioned in a location that is located overcancellous bone tissue of the patient's humerus when the sizinginstrument is secured to the patient's humerus.
 34. The surgicalinstrument assembly of claim 31, wherein: the sizing instrument has anupper surface and a lower surface, each of the punch guide holes extendsfrom the upper surface to the lower surface, the sizing instrumentfurther includes a number of bone-engaging spikes extending downwardlyfrom its lower surface, and each of the number of bone-engaging spikesis positioned in a location to engage cancellous bone tissue of thepatient's humerus when the sizing instrument is secured to the patient'shumerus.
 35. The surgical instrument assembly of claim 31, wherein eachof the punch guide holes of the sizing instrument is generally T-shaped.36. The surgical instrument assembly of claim 31, wherein: the roundbody of the sizing instrument is generally dome-shaped having aflattened upper surface and a planar opposite, lower surface, anelongated drill guide bore extends through a center of the sizinginstrument from the upper surface to the lower surface, and the drillguide bore is positioned in a location that is located over cancellousbone tissue of the patient's humerus when the sizing instrument issecured to the patient's humerus.
 37. The surgical instrument assemblyof claim 31, further comprising a surgical punch configured to punchholes in the cancellous bone tissue of the patient's humerus to receivethe plurality of legs of the stemless humeral component, wherein: thesurgical punch comprises a plurality of tines, and each of the pluralityof tines of the surgical punch is positioned in a location that alignswith one of the punch guide holes of the sizing instrument.
 38. Thesurgical instrument assembly of claim 31, wherein: the trial headcomponent further comprises a center lug extending laterally away fromthe underside surface, and the center lug is configured to befrictionally secured to the sizing instrument when the center lug isinserted into an elongated drill guide bore extending through a centerof the sizing instrument.